Canonical Allele Identifier: CA399789759

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374420C>T , CM000679.2:g.44374420C>T	GRCh38
NC_000017.10:g.42451788C>T , CM000679.1:g.42451788C>T	GRCh37
NC_000017.9:g.39807314C>T	NCBI36
NG_008331.1:g.20086G>A , LRG_479:g.20086G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.2994G>A MANE Select	NP_000410.2:p.Trp998Ter
ENST00000262407.6:c.2994G>A MANE Select	ENSP00000262407.5:p.Trp998Ter
NM_000419.3:c.2994G>A , LRG_479t1:c.2994G>A	NP_000410.2:p.Trp998Ter
NM_000419.4:c.2994G>A	NP_000410.2:p.Trp998Ter
ENST00000262407.5:c.2994G>A	ENSP00000262407.5:p.Trp998Ter
ENST00000587295.5:c.253+1413G>A
ENST00000588098.1:c.37+239G>A
ENST00000592462.5:n.2693G>A
ENST00000648408.1:c.2374+239G>A
XM_011524749.1:c.2892G>A	XP_011523051.1:p.Trp964Ter
XM_011524750.1:c.2943+239G>A	XP_011523052.1:n.2943+239G>A