Canonical Allele Identifier: CA694990117

Gene: IRS2

Linked Data

• dbSNP Id: rs1466098073
• gnomAD v3: 13-109767145-C-G
• gnomAD v4: 13-109767145-C-G
• MyVariant Identifiers: chr13:g.110419492C>G (hg19) ; chr13:g.109767145C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.109767145C>G , CM000675.2:g.109767145C>G	GRCh38
NC_000013.10:g.110419492C>G , CM000675.1:g.110419492C>G	GRCh37
NC_000013.9:g.109217493C>G	NCBI36
NG_008154.1:g.24423G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375856.5:c.4013-10837G>C MANE Select	ENSP00000365016.3:n.4013-10837G>C
ENST00000375856.4:c.4013-10837G>C	ENSP00000365016.3:n.4013-10837G>C
NM_003749.2:c.4013-10837G>C	NP_003740.2:n.4013-10837G>C
NM_003749.3:c.4013-10837G>C MANE Select	NP_003740.2:n.4013-10837G>C