Canonical Allele Identifier: CA2716767073
Gene: WRN HGNC NCBI

Linked Data

dbSNP Id: rs1811327901
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31033747G>A , CM000670.2:g.31033747G>A GRCh38
NC_000008.10:g.30891263G>A , CM000670.1:g.30891263G>A GRCh37
NC_000008.9:g.31010805G>A NCBI36
NG_008870.1:g.5486G>A , LRG_524:g.5486G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000553.4:c.-303G>A , LRG_524t1:c.-303G>A NP_000544.2:n.-303G>A
NM_000553.5:c.-303G>A NP_000544.2:n.-303G>A
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