Canonical Allele Identifier: CA694990098

Gene: IRS2

Linked Data

• dbSNP Id: rs1195197209
• gnomAD v3: 13-109767073-G-C
• gnomAD v4: 13-109767073-G-C
• MyVariant Identifiers: chr13:g.110419420G>C (hg19) ; chr13:g.109767073G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.109767073G>C , CM000675.2:g.109767073G>C	GRCh38
NC_000013.10:g.110419420G>C , CM000675.1:g.110419420G>C	GRCh37
NC_000013.9:g.109217421G>C	NCBI36
NG_008154.1:g.24495C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375856.5:c.4013-10765C>G MANE Select	ENSP00000365016.3:n.4013-10765C>G
ENST00000375856.4:c.4013-10765C>G	ENSP00000365016.3:n.4013-10765C>G
NM_003749.2:c.4013-10765C>G	NP_003740.2:n.4013-10765C>G
NM_003749.3:c.4013-10765C>G MANE Select	NP_003740.2:n.4013-10765C>G