Canonical Allele Identifier: CA256232359
Gene: IRS2 HGNC NCBI

Linked Data

dbSNP Id: rs911275723
gnomAD v2: 13-110419431-G-A
gnomAD v3: 13-109767084-G-A
gnomAD v4: 13-109767084-G-A
MyVariant Identifiers: chr13:g.110419431G>A (hg19) chr13:g.109767084G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.109767084G>A , CM000675.2:g.109767084G>A GRCh38
NC_000013.10:g.110419431G>A , CM000675.1:g.110419431G>A GRCh37
NC_000013.9:g.109217432G>A NCBI36
NG_008154.1:g.24484C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375856.5:c.4013-10776C>T MANE Select ENSP00000365016.3:n.4013-10776C>T
ENST00000375856.4:c.4013-10776C>T ENSP00000365016.3:n.4013-10776C>T
NM_003749.2:c.4013-10776C>T NP_003740.2:n.4013-10776C>T
NM_003749.3:c.4013-10776C>T MANE Select NP_003740.2:n.4013-10776C>T
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