Variants - The Globin Gene Server - Leiden Open Variation Database

The Globin Gene Server

G-gamma globin (HBG2)

LOVD v.2.0 Build 38 [ Current LOVD status ]
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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 (#0000579)
Disease	Hb variants
Reference	(OMIM 0037);dbSNP;SwissVar VAR_003137;Qualtieri A et al.;
Template	Protein
Technique	Amino
Remarks	Hb F-Cosenza
# Reported	1
Ethnic origin	-
Disease Mesh ID	C074594
Geographic origin	-

Variant data
Allele	Unknown
Reported pathogenicity	Probably pathogenic
Concluded pathogenicity	Unknown
Exon	1
DNA change	HBG2:c.77G>A (View in UCSC Genome Browser, Ensembl)
RNA change	-
Protein	p.Gly26Glu
Re-site	-
Frequency	-
DB-ID	HBG2_00579
HbVar link	HbVar

1 entry in HBG2

Path.

Allele

Exon

DNA change

RNA change

Protein

Re-site

Frequency

DB-ID

HbVar link

+?/?

Unknown

1

-

p.Gly26Glu

-

-

HBG2_00579