Canonical Allele Identifier: CA1435753436
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269478C= , CM000666.2:g.6269478C= GRCh38
NC_000004.11:g.6271205C= , CM000666.1:g.6271205C= GRCh37
NC_000004.10:g.6322106C= NCBI36
NG_011700.1:g.4629C=

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7839C= XP_016864075.1:n.4+7839C=