Canonical Allele Identifier: CA2261366853

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44377674G= , CM000679.2:g.44377674G=	GRCh38
NC_000017.10:g.42455042G= , CM000679.1:g.42455042G=	GRCh37
NC_000017.9:g.39810568G=	NCBI36
NG_008331.1:g.16832C= , LRG_479:g.16832C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2187+24C= MANE Select	ENSP00000262407.5:n.2187+24C=
ENST00000648408.1:c.1618+24C=
ENST00000262407.5:c.2187+24C=	ENSP00000262407.5:n.2187+24C=
ENST00000592462.5:n.982+24C=
NM_000419.3:c.2187+24C= , LRG_479t1:c.2187+24C=	NP_000410.2:n.2187+24C=
XM_011524749.1:c.2187+24C=	XP_011523051.1:n.2187+24C=
XM_011524750.1:c.2187+24C=	XP_011523052.1:n.2187+24C=
NM_000419.4:c.2187+24C=	NP_000410.2:n.2187+24C=
NM_000419.5:c.2187+24C= MANE Select	NP_000410.2:n.2187+24C=