Canonical Allele Identifier: CA2686834098
Gene: WRN HGNC NCBI

Linked Data

gnomAD v4: 8-31033668-GCGGGGCTGGATGGGCTGTGGTGGGAGGGTTGCAGCGCCGCGAGAAAGGCGAGCCGGGCCGGGGGCGGGGAAAGGGGTGGGGCAGGAACGGGGGCGGGGA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31033672_31033770del , CM000670.2:g.31033672_31033770del GRCh38
NC_000008.10:g.30891188_30891286del , CM000670.1:g.30891188_30891286del GRCh37
NC_000008.9:g.31010730_31010828del NCBI36
NG_008870.1:g.5411_5509del , LRG_524:g.5411_5509del

Transcript Alleles

HGVS Amino-acid Change
NM_000553.4:c.-378_-280del , LRG_524t1:c.-378_-280del NP_000544.2:n.-378_-280del
NM_000553.5:c.-378_-280del NP_000544.2:n.-378_-280del
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