Canonical Allele Identifier: CA2686834124
Gene: WRN HGNC NCBI

Linked Data

gnomAD v4: 8-31033763-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31033763G>A , CM000670.2:g.31033763G>A GRCh38
NC_000008.10:g.30891279G>A , CM000670.1:g.30891279G>A GRCh37
NC_000008.9:g.31010821G>A NCBI36
NG_008870.1:g.5502G>A , LRG_524:g.5502G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000553.4:c.-287G>A , LRG_524t1:c.-287G>A NP_000544.2:n.-287G>A
NM_000553.5:c.-287G>A NP_000544.2:n.-287G>A
XM_011544639.3:c.-287G>A XP_011542941.1:n.-287G>A
XR_949470.3:n.15G>A
XR_949471.3:n.15G>A
XR_949472.3:n.15G>A