Canonical Allele Identifier: CA2261369846

Gene: ITGA2B

Linked Data

• dbSNP Id: rs911147845
• gnomAD v4: 17-44384226-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384226G>A , CM000679.2:g.44384226G>A	GRCh38
NC_000017.10:g.42461594G>A , CM000679.1:g.42461594G>A	GRCh37
NC_000017.9:g.39817120G>A	NCBI36
NG_008331.1:g.10280C>T , LRG_479:g.10280C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.891+85C>T MANE Select	ENSP00000262407.5:n.891+85C>T
ENST00000648408.1:c.322+85C>T
ENST00000262407.5:c.891+85C>T	ENSP00000262407.5:n.891+85C>T
ENST00000589645.5:n.342+85C>T
ENST00000591990.5:n.436+85C>T
ENST00000592075.5:n.260+85C>T
ENST00000592226.5:n.131+85C>T
ENST00000592253.5:n.399+85C>T
NM_000419.3:c.891+85C>T , LRG_479t1:c.891+85C>T	NP_000410.2:n.891+85C>T
XM_011524749.1:c.891+85C>T	XP_011523051.1:n.891+85C>T
XM_011524750.1:c.891+85C>T	XP_011523052.1:n.891+85C>T
NM_000419.4:c.891+85C>T	NP_000410.2:n.891+85C>T
NM_000419.5:c.891+85C>T MANE Select	NP_000410.2:n.891+85C>T