Canonical Allele Identifier: CA1435753448
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269510C= , CM000666.2:g.6269510C= GRCh38
NC_000004.11:g.6271237C= , CM000666.1:g.6271237C= GRCh37
NC_000004.10:g.6322138C= NCBI36
NG_011700.1:g.4661C=

Transcript Alleles

HGVS Amino-acid Change
XM_017008586.1:c.4+7871C= XP_016864075.1:n.4+7871C=