Canonical Allele Identifier: CA2118539313
Gene: IRS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.109767074G= , CM000675.2:g.109767074G= GRCh38
NC_000013.10:g.110419421G= , CM000675.1:g.110419421G= GRCh37
NC_000013.9:g.109217422G= NCBI36
NG_008154.1:g.24494C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375856.5:c.4013-10766C= MANE Select ENSP00000365016.3:n.4013-10766C=
ENST00000375856.4:c.4013-10766C= ENSP00000365016.3:n.4013-10766C=
NM_003749.2:c.4013-10766C= NP_003740.2:n.4013-10766C=
NM_003749.3:c.4013-10766C= MANE Select NP_003740.2:n.4013-10766C=
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