Canonical Allele Identifier: CA772285312

Gene: ITGA2B

Linked Data

• dbSNP Id: rs372198109
• gnomAD v3: 17-44374617-G-T
• gnomAD v4: 17-44374617-G-T
• MyVariant Identifiers: chr17:g.42451985G>T (hg19) ; chr17:g.44374617G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374617G>T , CM000679.2:g.44374617G>T	GRCh38
NC_000017.10:g.42451985G>T , CM000679.1:g.42451985G>T	GRCh37
NC_000017.9:g.39807511G>T	NCBI36
NG_008331.1:g.19889C>A , LRG_479:g.19889C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2943+42C>A MANE Select	ENSP00000262407.5:n.2943+42C>A
ENST00000648408.1:c.2374+42C>A
ENST00000262407.5:c.2943+42C>A	ENSP00000262407.5:n.2943+42C>A
ENST00000587295.5:c.253+1216C>A
ENST00000588098.1:c.37+42C>A
ENST00000592462.5:n.2496C>A
NM_000419.3:c.2943+42C>A , LRG_479t1:c.2943+42C>A	NP_000410.2:n.2943+42C>A
XM_011524749.1:c.2842-147C>A	XP_011523051.1:n.2842-147C>A
XM_011524750.1:c.2943+42C>A	XP_011523052.1:n.2943+42C>A
NM_000419.4:c.2943+42C>A	NP_000410.2:n.2943+42C>A
NM_000419.5:c.2943+42C>A MANE Select	NP_000410.2:n.2943+42C>A