Canonical Allele Identifier: CA694990097

Gene: IRS2

Linked Data

• dbSNP Id: rs1371280722
• gnomAD v3: 13-109767062-T-A
• gnomAD v4: 13-109767062-T-A
• MyVariant Identifiers: chr13:g.110419409T>A (hg19) ; chr13:g.109767062T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.109767062T>A , CM000675.2:g.109767062T>A	GRCh38
NC_000013.10:g.110419409T>A , CM000675.1:g.110419409T>A	GRCh37
NC_000013.9:g.109217410T>A	NCBI36
NG_008154.1:g.24506A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375856.5:c.4013-10754A>T MANE Select	ENSP00000365016.3:n.4013-10754A>T
ENST00000375856.4:c.4013-10754A>T	ENSP00000365016.3:n.4013-10754A>T
NM_003749.2:c.4013-10754A>T	NP_003740.2:n.4013-10754A>T
NM_003749.3:c.4013-10754A>T MANE Select	NP_003740.2:n.4013-10754A>T