Canonical Allele Identifier: CA2261365730

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375380A= , CM000679.2:g.44375380A=	GRCh38
NC_000017.10:g.42452748A= , CM000679.1:g.42452748A=	GRCh37
NC_000017.9:g.39808274A=	NCBI36
NG_008331.1:g.19126T= , LRG_479:g.19126T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2727+211T= MANE Select	ENSP00000262407.5:n.2727+211T=
ENST00000648408.1:c.2158+211T=
ENST00000262407.5:c.2727+211T=	ENSP00000262407.5:n.2727+211T=
ENST00000587295.5:c.253+453T=
ENST00000592462.5:n.1733T=
NM_000419.3:c.2727+211T= , LRG_479t1:c.2727+211T=	NP_000410.2:n.2727+211T=
XM_011524749.1:c.2727+211T=	XP_011523051.1:n.2727+211T=
XM_011524750.1:c.2727+211T=	XP_011523052.1:n.2727+211T=
NM_000419.4:c.2727+211T=	NP_000410.2:n.2727+211T=
NM_000419.5:c.2727+211T= MANE Select	NP_000410.2:n.2727+211T=