Canonical Allele Identifier: CA399805350

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42462401G>T (hg19) ; chr17:g.44385033G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.714C>A MANE Select	ENSP00000262407.5:p.Tyr238Ter
ENST00000648408.1:c.145C>A
ENST00000262407.5:c.714C>A	ENSP00000262407.5:p.Tyr238Ter
ENST00000589645.5:n.165C>A
ENST00000591990.5:n.76C>A
ENST00000592075.5:n.83C>A
ENST00000592226.5:n.39+131C>A
ENST00000592253.5:n.222C>A
ENST00000592944.1:n.396C>A
NM_000419.3:c.714C>A , LRG_479t1:c.714C>A	NP_000410.2:p.Tyr238Ter
XM_011524749.1:c.714C>A	XP_011523051.1:p.Tyr238Ter
XM_011524750.1:c.714C>A	XP_011523052.1:p.Tyr238Ter
NM_000419.4:c.714C>A	NP_000410.2:p.Tyr238Ter
NM_000419.5:c.714C>A MANE Select	NP_000410.2:p.Tyr238Ter