Canonical Allele Identifier: CA2261365331
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374636C= , CM000679.2:g.44374636C= GRCh38
NC_000017.10:g.42452004C= , CM000679.1:g.42452004C= GRCh37
NC_000017.9:g.39807530C= NCBI36
NG_008331.1:g.19870G= , LRG_479:g.19870G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2943+23G= MANE Select ENSP00000262407.5:n.2943+23G=
ENST00000648408.1:c.2374+23G=
ENST00000262407.5:c.2943+23G= ENSP00000262407.5:n.2943+23G=
ENST00000587295.5:c.253+1197G=
ENST00000588098.1:c.37+23G=
ENST00000592462.5:n.2477G=
NM_000419.3:c.2943+23G= , LRG_479t1:c.2943+23G= NP_000410.2:n.2943+23G=
XM_011524749.1:c.2842-166G= XP_011523051.1:n.2842-166G=
XM_011524750.1:c.2943+23G= XP_011523052.1:n.2943+23G=
NM_000419.4:c.2943+23G= NP_000410.2:n.2943+23G=
NM_000419.5:c.2943+23G= MANE Select NP_000410.2:n.2943+23G=