Canonical Allele Identifier: CA2261364428

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372514C= , CM000679.2:g.44372514C=	GRCh38
NC_000017.10:g.42449882C= , CM000679.1:g.42449882C=	GRCh37
NC_000017.9:g.39805408C=	NCBI36
NG_008331.1:g.21992G= , LRG_479:g.21992G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.3061-91G= MANE Select	ENSP00000262407.5:n.3061-91G=
ENST00000648408.1:c.2375-91G=
ENST00000262407.5:c.3061-91G=	ENSP00000262407.5:n.3061-91G=
ENST00000587295.5:c.254-91G=
ENST00000588098.1:c.38-91G=
NM_000419.3:c.3061-91G= , LRG_479t1:c.3061-91G=	NP_000410.2:n.3061-91G=
XM_011524749.1:c.2959-91G=	XP_011523051.1:n.2959-91G=
XM_011524750.1:c.2944-91G=	XP_011523052.1:n.2944-91G=
NM_000419.4:c.3061-91G=	NP_000410.2:n.3061-91G=
NM_000419.5:c.3061-91G= MANE Select	NP_000410.2:n.3061-91G=