Canonical Allele Identifier: CA1112367178
Gene: WRN HGNC NCBI

Linked Data

dbSNP Id: rs1585375388
gnomAD v3: 8-31033766-G-A
gnomAD v4: 8-31033766-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31033766G>A , CM000670.2:g.31033766G>A GRCh38
NC_000008.10:g.30891282G>A , CM000670.1:g.30891282G>A GRCh37
NC_000008.9:g.31010824G>A NCBI36
NG_008870.1:g.5505G>A , LRG_524:g.5505G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000553.4:c.-284G>A , LRG_524t1:c.-284G>A NP_000544.2:n.-284G>A
NM_000553.5:c.-284G>A NP_000544.2:n.-284G>A
XM_011544639.3:c.-284G>A XP_011542941.1:n.-284G>A
XR_949470.3:n.18G>A
XR_949471.3:n.18G>A
XR_949472.3:n.18G>A
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