Canonical Allele Identifier: CA1058877214
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1729730491
gnomAD v3: 4-6269465-C-G
gnomAD v4: 4-6269465-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269465C>G , CM000666.2:g.6269465C>G GRCh38
NC_000004.11:g.6271192C>G , CM000666.1:g.6271192C>G GRCh37
NC_000004.10:g.6322093C>G NCBI36
NG_011700.1:g.4616C>G

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7826C>G XP_016864075.1:n.4+7826C>G