Canonical Allele Identifier: CA1435753390
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1729728663

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269398C>T , CM000666.2:g.6269398C>T GRCh38
NC_000004.11:g.6271125C>T , CM000666.1:g.6271125C>T GRCh37
NC_000004.10:g.6322026C>T NCBI36
NG_011700.1:g.4549C>T

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7759C>T XP_016864075.1:n.4+7759C>T