Canonical Allele Identifier: CA2261370315

Gene: ITGA2B

Linked Data

• dbSNP Id: rs2048633275
• gnomAD v4: 17-44385145-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385145T>G , CM000679.2:g.44385145T>G	GRCh38
NC_000017.10:g.42462513T>G , CM000679.1:g.42462513T>G	GRCh37
NC_000017.9:g.39818039T>G	NCBI36
NG_008331.1:g.9361A>C , LRG_479:g.9361A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.670+19A>C MANE Select	ENSP00000262407.5:n.670+19A>C
ENST00000648408.1:c.101+19A>C
ENST00000262407.5:c.670+19A>C	ENSP00000262407.5:n.670+19A>C
ENST00000589645.5:n.121+19A>C
ENST00000591990.5:n.32+19A>C
ENST00000592075.5:n.39+19A>C
ENST00000592226.5:n.39+19A>C
ENST00000592253.5:n.178+19A>C
ENST00000592944.1:n.352+19A>C
NM_000419.3:c.670+19A>C , LRG_479t1:c.670+19A>C	NP_000410.2:n.670+19A>C
XM_011524749.1:c.670+19A>C	XP_011523051.1:n.670+19A>C
XM_011524750.1:c.670+19A>C	XP_011523052.1:n.670+19A>C
NM_000419.4:c.670+19A>C	NP_000410.2:n.670+19A>C
NM_000419.5:c.670+19A>C MANE Select	NP_000410.2:n.670+19A>C