Canonical Allele Identifier: CA2261365309
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374596G= , CM000679.2:g.44374596G= GRCh38
NC_000017.10:g.42451964G= , CM000679.1:g.42451964G= GRCh37
NC_000017.9:g.39807490G= NCBI36
NG_008331.1:g.19910C= , LRG_479:g.19910C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2943+63C= MANE Select ENSP00000262407.5:n.2943+63C=
ENST00000648408.1:c.2374+63C=
ENST00000262407.5:c.2943+63C= ENSP00000262407.5:n.2943+63C=
ENST00000587295.5:c.253+1237C=
ENST00000588098.1:c.37+63C=
ENST00000592462.5:n.2517C=
NM_000419.3:c.2943+63C= , LRG_479t1:c.2943+63C= NP_000410.2:n.2943+63C=
XM_011524749.1:c.2842-126C= XP_011523051.1:n.2842-126C=
XM_011524750.1:c.2943+63C= XP_011523052.1:n.2943+63C=
NM_000419.4:c.2943+63C= NP_000410.2:n.2943+63C=
NM_000419.5:c.2943+63C= MANE Select NP_000410.2:n.2943+63C=
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