Canonical Allele Identifier: CA1435753408
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs13127445

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269423C>A , CM000666.2:g.6269423C>A GRCh38
NC_000004.11:g.6271150C>A , CM000666.1:g.6271150C>A GRCh37
NC_000004.10:g.6322051C>A NCBI36
NG_011700.1:g.4574C>A

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7784C>A XP_016864075.1:n.4+7784C>A