Canonical Allele Identifier: CA2261368361

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44380915G= , CM000679.2:g.44380915G=	GRCh38
NC_000017.10:g.42458283G= , CM000679.1:g.42458283G=	GRCh37
NC_000017.9:g.39813809G=	NCBI36
NG_008331.1:g.13591C= , LRG_479:g.13591C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.1357C= MANE Select	ENSP00000262407.5:p.Arg453=
ENST00000648408.1:c.788C=
ENST00000262407.5:c.1357C=	ENSP00000262407.5:p.Arg453=
ENST00000592226.5:n.597C=
ENST00000592462.5:n.152C=
NM_000419.3:c.1357C= , LRG_479t1:c.1357C=	NP_000410.2:p.Arg453=
XM_011524749.1:c.1357C=	XP_011523051.1:p.Arg453=
XM_011524750.1:c.1357C=	XP_011523052.1:p.Arg453=
NM_000419.4:c.1357C=	NP_000410.2:p.Arg453=
NM_000419.5:c.1357C= MANE Select	NP_000410.2:p.Arg453=