Canonical Allele Identifier: CA850706346
Gene: WRN HGNC NCBI

Linked Data

dbSNP Id: rs1304378045
gnomAD v3: 8-31033774-T-G
gnomAD v4: 8-31033774-T-G
MyVariant Identifiers: chr8:g.30891290T>G (hg19) chr8:g.31033774T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31033774T>G , CM000670.2:g.31033774T>G GRCh38
NC_000008.10:g.30891290T>G , CM000670.1:g.30891290T>G GRCh37
NC_000008.9:g.31010832T>G NCBI36
NG_008870.1:g.5513T>G , LRG_524:g.5513T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000553.4:c.-276T>G , LRG_524t1:c.-276T>G NP_000544.2:n.-276T>G
NM_000553.5:c.-276T>G NP_000544.2:n.-276T>G
XM_011544639.3:c.-276T>G XP_011542941.1:n.-276T>G
XR_949470.3:n.26T>G
XR_949471.3:n.26T>G
XR_949472.3:n.26T>G
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