Canonical Allele Identifier: CA2261365368

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374694C= , CM000679.2:g.44374694C=	GRCh38
NC_000017.10:g.42452062C= , CM000679.1:g.42452062C=	GRCh37
NC_000017.9:g.39807588C=	NCBI36
NG_008331.1:g.19812G= , LRG_479:g.19812G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2908G= MANE Select	ENSP00000262407.5:p.Val970=
ENST00000648408.1:c.2339G=
ENST00000262407.5:c.2908G=	ENSP00000262407.5:p.Val970=
ENST00000587295.5:c.253+1139G=
ENST00000588098.1:c.2G=
ENST00000592462.5:n.2419G=
NM_000419.3:c.2908G= , LRG_479t1:c.2908G=	NP_000410.2:p.Val970=
XM_011524749.1:c.2842-224G=	XP_011523051.1:n.2842-224G=
XM_011524750.1:c.2908G=	XP_011523052.1:p.Val970=
NM_000419.4:c.2908G=	NP_000410.2:p.Val970=
NM_000419.5:c.2908G= MANE Select	NP_000410.2:p.Val970=