Canonical Allele Identifier: CA2261364387

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372440G= , CM000679.2:g.44372440G=	GRCh38
NC_000017.10:g.42449808G= , CM000679.1:g.42449808G=	GRCh37
NC_000017.9:g.39805334G=	NCBI36
NG_008331.1:g.22066C= , LRG_479:g.22066C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.3061-17C= MANE Select	ENSP00000262407.5:n.3061-17C=
ENST00000648408.1:c.2375-17C=
ENST00000262407.5:c.3061-17C=	ENSP00000262407.5:n.3061-17C=
ENST00000587295.5:c.254-17C=
ENST00000588098.1:c.38-17C=
NM_000419.3:c.3061-17C= , LRG_479t1:c.3061-17C=	NP_000410.2:n.3061-17C=
XM_011524749.1:c.2959-17C=	XP_011523051.1:n.2959-17C=
XM_011524750.1:c.2944-17C=	XP_011523052.1:n.2944-17C=
NM_000419.4:c.3061-17C=	NP_000410.2:n.3061-17C=
NM_000419.5:c.3061-17C= MANE Select	NP_000410.2:n.3061-17C=