Canonical Allele Identifier: CA2118539326
Gene: IRS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.109767105G= , CM000675.2:g.109767105G= GRCh38
NC_000013.10:g.110419452G= , CM000675.1:g.110419452G= GRCh37
NC_000013.9:g.109217453G= NCBI36
NG_008154.1:g.24463C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375856.5:c.4013-10797C= MANE Select ENSP00000365016.3:n.4013-10797C=
ENST00000375856.4:c.4013-10797C= ENSP00000365016.3:n.4013-10797C=
NM_003749.2:c.4013-10797C= NP_003740.2:n.4013-10797C=
NM_003749.3:c.4013-10797C= MANE Select NP_003740.2:n.4013-10797C=