Canonical Allele Identifier: CA2261364408

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372483A= , CM000679.2:g.44372483A=	GRCh38
NC_000017.10:g.42449851A= , CM000679.1:g.42449851A=	GRCh37
NC_000017.9:g.39805377A=	NCBI36
NG_008331.1:g.22023T= , LRG_479:g.22023T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.3061-60T= MANE Select	ENSP00000262407.5:n.3061-60T=
ENST00000648408.1:c.2375-60T=
ENST00000262407.5:c.3061-60T=	ENSP00000262407.5:n.3061-60T=
ENST00000587295.5:c.254-60T=
ENST00000588098.1:c.38-60T=
NM_000419.3:c.3061-60T= , LRG_479t1:c.3061-60T=	NP_000410.2:n.3061-60T=
XM_011524749.1:c.2959-60T=	XP_011523051.1:n.2959-60T=
XM_011524750.1:c.2944-60T=	XP_011523052.1:n.2944-60T=
NM_000419.4:c.3061-60T=	NP_000410.2:n.3061-60T=
NM_000419.5:c.3061-60T= MANE Select	NP_000410.2:n.3061-60T=