Canonical Allele Identifier: CA2261369835

Gene: ITGA2B

Linked Data

• dbSNP Id: rs1598382044
• gnomAD v4: 17-44384210-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384210T>G , CM000679.2:g.44384210T>G	GRCh38
NC_000017.10:g.42461578T>G , CM000679.1:g.42461578T>G	GRCh37
NC_000017.9:g.39817104T>G	NCBI36
NG_008331.1:g.10296A>C , LRG_479:g.10296A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.892-72A>C MANE Select	ENSP00000262407.5:n.892-72A>C
ENST00000648408.1:c.323-72A>C
ENST00000262407.5:c.892-72A>C	ENSP00000262407.5:n.892-72A>C
ENST00000589645.5:n.343-72A>C
ENST00000591990.5:n.437-72A>C
ENST00000592075.5:n.261-72A>C
ENST00000592226.5:n.132-72A>C
ENST00000592253.5:n.400-72A>C
NM_000419.3:c.892-72A>C , LRG_479t1:c.892-72A>C	NP_000410.2:n.892-72A>C
XM_011524749.1:c.892-72A>C	XP_011523051.1:n.892-72A>C
XM_011524750.1:c.892-72A>C	XP_011523052.1:n.892-72A>C
NM_000419.4:c.892-72A>C	NP_000410.2:n.892-72A>C
NM_000419.5:c.892-72A>C MANE Select	NP_000410.2:n.892-72A>C