Canonical Allele Identifier: CA1435753341
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1729727002

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269318G>A , CM000666.2:g.6269318G>A GRCh38
NC_000004.11:g.6271045G>A , CM000666.1:g.6271045G>A GRCh37
NC_000004.10:g.6321946G>A NCBI36
NG_011700.1:g.4469G>A

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7679G>A XP_016864075.1:n.4+7679G>A