Canonical Allele Identifier: CA2261365329
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374627G= , CM000679.2:g.44374627G= GRCh38
NC_000017.10:g.42451995G= , CM000679.1:g.42451995G= GRCh37
NC_000017.9:g.39807521G= NCBI36
NG_008331.1:g.19879C= , LRG_479:g.19879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2943+32C= MANE Select ENSP00000262407.5:n.2943+32C=
ENST00000648408.1:c.2374+32C=
ENST00000262407.5:c.2943+32C= ENSP00000262407.5:n.2943+32C=
ENST00000587295.5:c.253+1206C=
ENST00000588098.1:c.37+32C=
ENST00000592462.5:n.2486C=
NM_000419.3:c.2943+32C= , LRG_479t1:c.2943+32C= NP_000410.2:n.2943+32C=
XM_011524749.1:c.2842-157C= XP_011523051.1:n.2842-157C=
XM_011524750.1:c.2943+32C= XP_011523052.1:n.2943+32C=
NM_000419.4:c.2943+32C= NP_000410.2:n.2943+32C=
NM_000419.5:c.2943+32C= MANE Select NP_000410.2:n.2943+32C=
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