Canonical Allele Identifier: CA1058877101
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs766334562
gnomAD v3: 4-6269405-G-C
gnomAD v4: 4-6269405-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269405G>C , CM000666.2:g.6269405G>C GRCh38
NC_000004.11:g.6271132G>C , CM000666.1:g.6271132G>C GRCh37
NC_000004.10:g.6322033G>C NCBI36
NG_011700.1:g.4556G>C

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7766G>C XP_016864075.1:n.4+7766G>C