Canonical Allele Identifier: CA91777167
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs955852025

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269493G>A , CM000666.2:g.6269493G>A GRCh38
NC_000004.11:g.6271220G>A , CM000666.1:g.6271220G>A GRCh37
NC_000004.10:g.6322121G>A NCBI36
NG_011700.1:g.4644G>A

Transcript Alleles

HGVS Amino-acid Change
XM_017008586.1:c.4+7854G>A XP_016864075.1:n.4+7854G>A