Canonical Allele Identifier: CA500280156

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42462401G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385033G>A , CM000679.2:g.44385033G>A	GRCh38
NC_000017.10:g.42462401G>A , CM000679.1:g.42462401G>A	GRCh37
NC_000017.9:g.39817927G>A	NCBI36
NG_008331.1:g.9473C>T , LRG_479:g.9473C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.714C>T MANE Select	ENSP00000262407.5:p.Tyr238=
ENST00000648408.1:c.145C>T
ENST00000262407.5:c.714C>T	ENSP00000262407.5:p.Tyr238=
ENST00000589645.5:n.165C>T
ENST00000591990.5:n.76C>T
ENST00000592075.5:n.83C>T
ENST00000592226.5:n.39+131C>T
ENST00000592253.5:n.222C>T
ENST00000592944.1:n.396C>T
NM_000419.3:c.714C>T , LRG_479t1:c.714C>T	NP_000410.2:p.Tyr238=
XM_011524749.1:c.714C>T	XP_011523051.1:p.Tyr238=
XM_011524750.1:c.714C>T	XP_011523052.1:p.Tyr238=
NM_000419.4:c.714C>T	NP_000410.2:p.Tyr238=
NM_000419.5:c.714C>T MANE Select	NP_000410.2:p.Tyr238=