Canonical Allele Identifier: CA399805116

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42461936C>T (hg19) ; chr17:g.44384568C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384568C>T , CM000679.2:g.44384568C>T	GRCh38
NC_000017.10:g.42461936C>T , CM000679.1:g.42461936C>T	GRCh37
NC_000017.9:g.39817462C>T	NCBI36
NG_008331.1:g.9938G>A , LRG_479:g.9938G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.817G>A MANE Select	ENSP00000262407.5:p.Gly273Ser
ENST00000648408.1:c.248G>A
ENST00000262407.5:c.817G>A	ENSP00000262407.5:p.Gly273Ser
ENST00000589645.5:n.268G>A
ENST00000591990.5:n.179G>A
ENST00000592075.5:n.186G>A
ENST00000592226.5:n.57G>A
ENST00000592253.5:n.325G>A
ENST00000592944.1:n.499G>A
NM_000419.3:c.817G>A , LRG_479t1:c.817G>A	NP_000410.2:p.Gly273Ser
XM_011524749.1:c.817G>A	XP_011523051.1:p.Gly273Ser
XM_011524750.1:c.817G>A	XP_011523052.1:p.Gly273Ser
NM_000419.4:c.817G>A	NP_000410.2:p.Gly273Ser
NM_000419.5:c.817G>A MANE Select	NP_000410.2:p.Gly273Ser