Canonical Allele Identifier: CA797143915
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1334069783

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269474G>C , CM000666.2:g.6269474G>C GRCh38
NC_000004.11:g.6271201G>C , CM000666.1:g.6271201G>C GRCh37
NC_000004.10:g.6322102G>C NCBI36
NG_011700.1:g.4625G>C

Transcript Alleles

HGVS Amino-acid Change
XM_017008586.1:c.4+7835G>C XP_016864075.1:n.4+7835G>C