Canonical Allele Identifier: CA1435753358
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269343T= , CM000666.2:g.6269343T= GRCh38
NC_000004.11:g.6271070T= , CM000666.1:g.6271070T= GRCh37
NC_000004.10:g.6321971T= NCBI36
NG_011700.1:g.4494T=

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7704T= XP_016864075.1:n.4+7704T=