Canonical Allele Identifier: CA91777187
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs937501463
gnomAD v3: 4-6269519-T-G
gnomAD v4: 4-6269519-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269519T>G , CM000666.2:g.6269519T>G GRCh38
NC_000004.11:g.6271246T>G , CM000666.1:g.6271246T>G GRCh37
NC_000004.10:g.6322147T>G NCBI36
NG_011700.1:g.4670T>G

Transcript Alleles

HGVS Amino-acid Change
XM_017008586.1:c.4+7880T>G XP_016864075.1:n.4+7880T>G