Canonical Allele Identifier: CA13801511

Gene: IRS2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.109759221C>T , CM000675.2:g.109759221C>T	GRCh38
NC_000013.10:g.110411568C>T , CM000675.1:g.110411568C>T	GRCh37
NC_000013.9:g.109209569C>T	NCBI36
NG_008154.1:g.32347G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375856.5:c.4013-2913G>A MANE Select	ENSP00000365016.3:n.4013-2913G>A
ENST00000375856.4:c.4013-2913G>A	ENSP00000365016.3:n.4013-2913G>A
NM_003749.2:c.4013-2913G>A	NP_003740.2:n.4013-2913G>A
NM_003749.3:c.4013-2913G>A MANE Select	NP_003740.2:n.4013-2913G>A