Canonical Allele Identifier: CA2261370303

Gene: ITGA2B

Linked Data

• dbSNP Id: rs2048633011

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385126C>T , CM000679.2:g.44385126C>T	GRCh38
NC_000017.10:g.42462494C>T , CM000679.1:g.42462494C>T	GRCh37
NC_000017.9:g.39818020C>T	NCBI36
NG_008331.1:g.9380G>A , LRG_479:g.9380G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.670+38G>A MANE Select	ENSP00000262407.5:n.670+38G>A
ENST00000648408.1:c.101+38G>A
ENST00000262407.5:c.670+38G>A	ENSP00000262407.5:n.670+38G>A
ENST00000589645.5:n.121+38G>A
ENST00000591990.5:n.32+38G>A
ENST00000592075.5:n.39+38G>A
ENST00000592226.5:n.39+38G>A
ENST00000592253.5:n.178+38G>A
ENST00000592944.1:n.352+38G>A
NM_000419.3:c.670+38G>A , LRG_479t1:c.670+38G>A	NP_000410.2:n.670+38G>A
XM_011524749.1:c.670+38G>A	XP_011523051.1:n.670+38G>A
XM_011524750.1:c.670+38G>A	XP_011523052.1:n.670+38G>A
NM_000419.4:c.670+38G>A	NP_000410.2:n.670+38G>A
NM_000419.5:c.670+38G>A MANE Select	NP_000410.2:n.670+38G>A