Canonical Allele Identifier: CA500274065

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42458347C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44380979C>T , CM000679.2:g.44380979C>T	GRCh38
NC_000017.10:g.42458347C>T , CM000679.1:g.42458347C>T	GRCh37
NC_000017.9:g.39813873C>T	NCBI36
NG_008331.1:g.13527G>A , LRG_479:g.13527G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.1293G>A MANE Select	ENSP00000262407.5:p.Arg431=
ENST00000648408.1:c.724G>A
ENST00000262407.5:c.1293G>A	ENSP00000262407.5:p.Arg431=
ENST00000592226.5:n.533G>A
ENST00000592462.5:n.88G>A
NM_000419.3:c.1293G>A , LRG_479t1:c.1293G>A	NP_000410.2:p.Arg431=
XM_011524749.1:c.1293G>A	XP_011523051.1:p.Arg431=
XM_011524750.1:c.1293G>A	XP_011523052.1:p.Arg431=
NM_000419.4:c.1293G>A	NP_000410.2:p.Arg431=
NM_000419.5:c.1293G>A MANE Select	NP_000410.2:p.Arg431=