Canonical Allele Identifier: CA2591901972
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1017342810
gnomAD v3: 4-6269430-C-T
gnomAD v4: 4-6269430-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269430C>T , CM000666.2:g.6269430C>T GRCh38
NC_000004.11:g.6271157C>T , CM000666.1:g.6271157C>T GRCh37
NC_000004.10:g.6322058C>T NCBI36
NG_011700.1:g.4581C>T

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7791C>T XP_016864075.1:n.4+7791C>T