Canonical Allele Identifier: CA2118539272
Gene: IRS2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.109766982T= , CM000675.2:g.109766982T= GRCh38
NC_000013.10:g.110419329T= , CM000675.1:g.110419329T= GRCh37
NC_000013.9:g.109217330T= NCBI36
NG_008154.1:g.24586A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375856.5:c.4013-10674A= MANE Select ENSP00000365016.3:n.4013-10674A=
ENST00000375856.4:c.4013-10674A= ENSP00000365016.3:n.4013-10674A=
NM_003749.2:c.4013-10674A= NP_003740.2:n.4013-10674A=
NM_003749.3:c.4013-10674A= MANE Select NP_003740.2:n.4013-10674A=
Search 100 bp 5'
Search 100 bp 3'