Canonical Allele Identifier: CA694990067
Gene: IRS2 HGNC NCBI

Linked Data

dbSNP Id: rs1488380561
MyVariant Identifiers: chr13:g.110419319G>A (hg19) chr13:g.109766972G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.109766972G>A , CM000675.2:g.109766972G>A GRCh38
NC_000013.10:g.110419319G>A , CM000675.1:g.110419319G>A GRCh37
NC_000013.9:g.109217320G>A NCBI36
NG_008154.1:g.24596C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375856.5:c.4013-10664C>T MANE Select ENSP00000365016.3:n.4013-10664C>T
ENST00000375856.4:c.4013-10664C>T ENSP00000365016.3:n.4013-10664C>T
NM_003749.2:c.4013-10664C>T NP_003740.2:n.4013-10664C>T
NM_003749.3:c.4013-10664C>T MANE Select NP_003740.2:n.4013-10664C>T
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