Canonical Allele Identifier: CA694990114
Gene: IRS2 HGNC NCBI

Linked Data

dbSNP Id: rs1331906937

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.109767139G>C , CM000675.2:g.109767139G>C GRCh38
NC_000013.10:g.110419486G>C , CM000675.1:g.110419486G>C GRCh37
NC_000013.9:g.109217487G>C NCBI36
NG_008154.1:g.24429C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375856.5:c.4013-10831C>G MANE Select ENSP00000365016.3:n.4013-10831C>G
ENST00000375856.4:c.4013-10831C>G ENSP00000365016.3:n.4013-10831C>G
NM_003749.2:c.4013-10831C>G NP_003740.2:n.4013-10831C>G
NM_003749.3:c.4013-10831C>G MANE Select NP_003740.2:n.4013-10831C>G