Canonical Allele Identifier: CA2638214764

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374292-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374292G>T , CM000679.2:g.44374292G>T	GRCh38
NC_000017.10:g.42451660G>T , CM000679.1:g.42451660G>T	GRCh37
NC_000017.9:g.39807186G>T	NCBI36
NG_008331.1:g.20214C>A , LRG_479:g.20214C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.3060+62C>A MANE Select	ENSP00000262407.5:n.3060+62C>A
ENST00000648408.1:c.2374+367C>A
ENST00000262407.5:c.3060+62C>A	ENSP00000262407.5:n.3060+62C>A
ENST00000587295.5:c.253+1541C>A
ENST00000588098.1:c.37+367C>A
ENST00000592462.5:n.2821C>A
NM_000419.3:c.3060+62C>A , LRG_479t1:c.3060+62C>A	NP_000410.2:n.3060+62C>A
XM_011524749.1:c.2958+62C>A	XP_011523051.1:n.2958+62C>A
XM_011524750.1:c.2943+367C>A	XP_011523052.1:n.2943+367C>A
NM_000419.4:c.3060+62C>A	NP_000410.2:n.3060+62C>A
NM_000419.5:c.3060+62C>A MANE Select	NP_000410.2:n.3060+62C>A