Canonical Allele Identifier: CA2261366852

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44377673C= , CM000679.2:g.44377673C=	GRCh38
NC_000017.10:g.42455041C= , CM000679.1:g.42455041C=	GRCh37
NC_000017.9:g.39810567C=	NCBI36
NG_008331.1:g.16833G= , LRG_479:g.16833G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2187+25G= MANE Select	ENSP00000262407.5:n.2187+25G=
ENST00000648408.1:c.1618+25G=
ENST00000262407.5:c.2187+25G=	ENSP00000262407.5:n.2187+25G=
ENST00000592462.5:n.982+25G=
NM_000419.3:c.2187+25G= , LRG_479t1:c.2187+25G=	NP_000410.2:n.2187+25G=
XM_011524749.1:c.2187+25G=	XP_011523051.1:n.2187+25G=
XM_011524750.1:c.2187+25G=	XP_011523052.1:n.2187+25G=
NM_000419.4:c.2187+25G=	NP_000410.2:n.2187+25G=
NM_000419.5:c.2187+25G= MANE Select	NP_000410.2:n.2187+25G=