Canonical Allele Identifier: CA2261366843

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44377659C= , CM000679.2:g.44377659C=	GRCh38
NC_000017.10:g.42455027C= , CM000679.1:g.42455027C=	GRCh37
NC_000017.9:g.39810553C=	NCBI36
NG_008331.1:g.16847G= , LRG_479:g.16847G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2187+39G= MANE Select	ENSP00000262407.5:n.2187+39G=
ENST00000648408.1:c.1618+39G=
ENST00000262407.5:c.2187+39G=	ENSP00000262407.5:n.2187+39G=
ENST00000592462.5:n.982+39G=
NM_000419.3:c.2187+39G= , LRG_479t1:c.2187+39G=	NP_000410.2:n.2187+39G=
XM_011524749.1:c.2187+39G=	XP_011523051.1:n.2187+39G=
XM_011524750.1:c.2187+39G=	XP_011523052.1:n.2187+39G=
NM_000419.4:c.2187+39G=	NP_000410.2:n.2187+39G=
NM_000419.5:c.2187+39G= MANE Select	NP_000410.2:n.2187+39G=