Canonical Allele Identifier: CA2261365947

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375785G= , CM000679.2:g.44375785G=	GRCh38
NC_000017.10:g.42453153G= , CM000679.1:g.42453153G=	GRCh37
NC_000017.9:g.39808679G=	NCBI36
NG_008331.1:g.18721C= , LRG_479:g.18721C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2601+48C= MANE Select	ENSP00000262407.5:n.2601+48C=
ENST00000648408.1:c.2032+48C=
ENST00000262407.5:c.2601+48C=	ENSP00000262407.5:n.2601+48C=
ENST00000587295.5:c.253+48C=
ENST00000592462.5:n.1396+48C=
NM_000419.3:c.2601+48C= , LRG_479t1:c.2601+48C=	NP_000410.2:n.2601+48C=
XM_011524749.1:c.2601+48C=	XP_011523051.1:n.2601+48C=
XM_011524750.1:c.2601+48C=	XP_011523052.1:n.2601+48C=
NM_000419.4:c.2601+48C=	NP_000410.2:n.2601+48C=
NM_000419.5:c.2601+48C= MANE Select	NP_000410.2:n.2601+48C=