Canonical Allele Identifier: CA2261365420
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374803C= , CM000679.2:g.44374803C= GRCh38
NC_000017.10:g.42452171C= , CM000679.1:g.42452171C= GRCh37
NC_000017.9:g.39807697C= NCBI36
NG_008331.1:g.19703G= , LRG_479:g.19703G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2842-43G= MANE Select ENSP00000262407.5:n.2842-43G=
ENST00000648408.1:c.2273-43G=
ENST00000262407.5:c.2842-43G= ENSP00000262407.5:n.2842-43G=
ENST00000587295.5:c.253+1030G=
ENST00000592462.5:n.2310G=
NM_000419.3:c.2842-43G= , LRG_479t1:c.2842-43G= NP_000410.2:n.2842-43G=
XM_011524749.1:c.2841+195G= XP_011523051.1:n.2841+195G=
XM_011524750.1:c.2842-43G= XP_011523052.1:n.2842-43G=
NM_000419.4:c.2842-43G= NP_000410.2:n.2842-43G=
NM_000419.5:c.2842-43G= MANE Select NP_000410.2:n.2842-43G=