Canonical Allele Identifier: CA2576291341

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44384212-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384212G>T , CM000679.2:g.44384212G>T	GRCh38
NC_000017.10:g.42461580G>T , CM000679.1:g.42461580G>T	GRCh37
NC_000017.9:g.39817106G>T	NCBI36
NG_008331.1:g.10294C>A , LRG_479:g.10294C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.892-74C>A MANE Select	ENSP00000262407.5:n.892-74C>A
ENST00000648408.1:c.323-74C>A
ENST00000262407.5:c.892-74C>A	ENSP00000262407.5:n.892-74C>A
ENST00000589645.5:n.343-74C>A
ENST00000591990.5:n.437-74C>A
ENST00000592075.5:n.261-74C>A
ENST00000592226.5:n.132-74C>A
ENST00000592253.5:n.400-74C>A
NM_000419.3:c.892-74C>A , LRG_479t1:c.892-74C>A	NP_000410.2:n.892-74C>A
XM_011524749.1:c.892-74C>A	XP_011523051.1:n.892-74C>A
XM_011524750.1:c.892-74C>A	XP_011523052.1:n.892-74C>A
NM_000419.4:c.892-74C>A	NP_000410.2:n.892-74C>A
NM_000419.5:c.892-74C>A MANE Select	NP_000410.2:n.892-74C>A