Canonical Allele Identifier: CA2118539271
Gene: IRS2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.109766977T= , CM000675.2:g.109766977T= GRCh38
NC_000013.10:g.110419324T= , CM000675.1:g.110419324T= GRCh37
NC_000013.9:g.109217325T= NCBI36
NG_008154.1:g.24591A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375856.5:c.4013-10669A= MANE Select ENSP00000365016.3:n.4013-10669A=
ENST00000375856.4:c.4013-10669A= ENSP00000365016.3:n.4013-10669A=
NM_003749.2:c.4013-10669A= NP_003740.2:n.4013-10669A=
NM_003749.3:c.4013-10669A= MANE Select NP_003740.2:n.4013-10669A=
Search 100 bp 5'
Search 100 bp 3'