Canonical Allele Identifier: CA2261365174
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374300G= , CM000679.2:g.44374300G= GRCh38
NC_000017.10:g.42451668G= , CM000679.1:g.42451668G= GRCh37
NC_000017.9:g.39807194G= NCBI36
NG_008331.1:g.20206C= , LRG_479:g.20206C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3060+54C= MANE Select ENSP00000262407.5:n.3060+54C=
ENST00000648408.1:c.2374+359C=
ENST00000262407.5:c.3060+54C= ENSP00000262407.5:n.3060+54C=
ENST00000587295.5:c.253+1533C=
ENST00000588098.1:c.37+359C=
ENST00000592462.5:n.2813C=
NM_000419.3:c.3060+54C= , LRG_479t1:c.3060+54C= NP_000410.2:n.3060+54C=
XM_011524749.1:c.2958+54C= XP_011523051.1:n.2958+54C=
XM_011524750.1:c.2943+359C= XP_011523052.1:n.2943+359C=
NM_000419.4:c.3060+54C= NP_000410.2:n.3060+54C=
NM_000419.5:c.3060+54C= MANE Select NP_000410.2:n.3060+54C=