Canonical Allele Identifier: CA2261370261

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385032G= , CM000679.2:g.44385032G=	GRCh38
NC_000017.10:g.42462400G= , CM000679.1:g.42462400G=	GRCh37
NC_000017.9:g.39817926G=	NCBI36
NG_008331.1:g.9474C= , LRG_479:g.9474C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.715C= MANE Select	ENSP00000262407.5:p.Arg239=
ENST00000648408.1:c.146C=
ENST00000262407.5:c.715C=	ENSP00000262407.5:p.Arg239=
ENST00000589645.5:n.166C=
ENST00000591990.5:n.77C=
ENST00000592075.5:n.84C=
ENST00000592226.5:n.39+132C=
ENST00000592253.5:n.223C=
ENST00000592944.1:n.397C=
NM_000419.3:c.715C= , LRG_479t1:c.715C=	NP_000410.2:p.Arg239=
XM_011524749.1:c.715C=	XP_011523051.1:p.Arg239=
XM_011524750.1:c.715C=	XP_011523052.1:p.Arg239=
NM_000419.4:c.715C=	NP_000410.2:p.Arg239=
NM_000419.5:c.715C= MANE Select	NP_000410.2:p.Arg239=