Canonical Allele Identifier: CA850706331
Gene: WRN HGNC NCBI

Linked Data

dbSNP Id: rs1275346778
MyVariant Identifiers: chr8:g.30891275G>C (hg19) chr8:g.31033759G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31033759G>C , CM000670.2:g.31033759G>C GRCh38
NC_000008.10:g.30891275G>C , CM000670.1:g.30891275G>C GRCh37
NC_000008.9:g.31010817G>C NCBI36
NG_008870.1:g.5498G>C , LRG_524:g.5498G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000553.4:c.-291G>C , LRG_524t1:c.-291G>C NP_000544.2:n.-291G>C
NM_000553.5:c.-291G>C NP_000544.2:n.-291G>C
XM_011544639.3:c.-291G>C XP_011542941.1:n.-291G>C
XR_949470.3:n.11G>C
XR_949471.3:n.11G>C
XR_949472.3:n.11G>C
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