Canonical Allele Identifier: CA2261365292
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374555C= , CM000679.2:g.44374555C= GRCh38
NC_000017.10:g.42451923C= , CM000679.1:g.42451923C= GRCh37
NC_000017.9:g.39807449C= NCBI36
NG_008331.1:g.19951G= , LRG_479:g.19951G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2944-85G= MANE Select ENSP00000262407.5:n.2944-85G=
ENST00000648408.1:c.2374+104G=
ENST00000262407.5:c.2944-85G= ENSP00000262407.5:n.2944-85G=
ENST00000587295.5:c.253+1278G=
ENST00000588098.1:c.37+104G=
ENST00000592462.5:n.2558G=
NM_000419.3:c.2944-85G= , LRG_479t1:c.2944-85G= NP_000410.2:n.2944-85G=
XM_011524749.1:c.2842-85G= XP_011523051.1:n.2842-85G=
XM_011524750.1:c.2943+104G= XP_011523052.1:n.2943+104G=
NM_000419.4:c.2944-85G= NP_000410.2:n.2944-85G=
NM_000419.5:c.2944-85G= MANE Select NP_000410.2:n.2944-85G=