Variants - The Globin Gene Server - Leiden Open Variation Database

The Globin Gene Server

alpha-2 globin (HBA2)

LOVD v.2.0 Build 38 [ Current LOVD status ]
Register as submitter | Log in

Curators: Belinda Giardine and Joseph Borg

About this overview [Show]
This detailed view shows all details of the selected patient, including all variants reported in this patient. At the bottom of the page, all variants reported in this patient are listed, with the one you are looking at in bold. The link to the UCSC Genome Browser will show the browser zoomed in to the location of the selected variant.

Patient data (#0000298)
Disease	Hb variants
Reference	(OMIM 0037);dbSNP;dbSNP;SwissVar VAR_002749;Carstairs KC et al.;Schneider RG et al.;
Template	Protein
Technique	Amino
Remarks	Hb Fort Worth
# Reported	1
Ethnic origin	-
Disease Mesh ID	C046190
Geographic origin	-

Variant data
Allele	Unknown
Reported pathogenicity	Probably pathogenic
Concluded pathogenicity	Unknown
Exon	1
DNA change	HBA2:c.83A>G (View in UCSC Genome Browser, Ensembl)
RNA change	-
Protein	p.Glu28Gly
Re-site	-
Frequency	-
DB-ID	HBA2_00298
HbVar link	HbVar

1 entry in HBA2

Path.

Allele

Exon

DNA change

RNA change

Protein

Re-site

Frequency

DB-ID

HbVar link

+?/?

Unknown

1

-

p.Glu28Gly

-

-

HBA2_00298