Canonical Allele Identifier: CA960132795
Gene: IRS2 HGNC NCBI

Linked Data

dbSNP Id: rs1877351568
gnomAD v3: 13-109767069-G-A
gnomAD v4: 13-109767069-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.109767069G>A , CM000675.2:g.109767069G>A GRCh38
NC_000013.10:g.110419416G>A , CM000675.1:g.110419416G>A GRCh37
NC_000013.9:g.109217417G>A NCBI36
NG_008154.1:g.24499C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375856.5:c.4013-10761C>T MANE Select ENSP00000365016.3:n.4013-10761C>T
ENST00000375856.4:c.4013-10761C>T ENSP00000365016.3:n.4013-10761C>T
NM_003749.2:c.4013-10761C>T NP_003740.2:n.4013-10761C>T
NM_003749.3:c.4013-10761C>T MANE Select NP_003740.2:n.4013-10761C>T
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