Canonical Allele Identifier: CA91777159
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs976183501

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269446A>C , CM000666.2:g.6269446A>C GRCh38
NC_000004.11:g.6271173A>C , CM000666.1:g.6271173A>C GRCh37
NC_000004.10:g.6322074A>C NCBI36
NG_011700.1:g.4597A>C

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7807A>C XP_016864075.1:n.4+7807A>C