Canonical Allele Identifier: CA2261370292

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385102G= , CM000679.2:g.44385102G=	GRCh38
NC_000017.10:g.42462470G= , CM000679.1:g.42462470G=	GRCh37
NC_000017.9:g.39817996G=	NCBI36
NG_008331.1:g.9404C= , LRG_479:g.9404C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.671-26C= MANE Select	ENSP00000262407.5:n.671-26C=
ENST00000648408.1:c.102-26C=
ENST00000262407.5:c.671-26C=	ENSP00000262407.5:n.671-26C=
ENST00000589645.5:n.122-26C=
ENST00000591990.5:n.33-26C=
ENST00000592075.5:n.40-26C=
ENST00000592226.5:n.39+62C=
ENST00000592253.5:n.179-26C=
ENST00000592944.1:n.353-26C=
NM_000419.3:c.671-26C= , LRG_479t1:c.671-26C=	NP_000410.2:n.671-26C=
XM_011524749.1:c.671-26C=	XP_011523051.1:n.671-26C=
XM_011524750.1:c.671-26C=	XP_011523052.1:n.671-26C=
NM_000419.4:c.671-26C=	NP_000410.2:n.671-26C=
NM_000419.5:c.671-26C= MANE Select	NP_000410.2:n.671-26C=