Canonical Allele Identifier: CA1435753369
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269367C= , CM000666.2:g.6269367C= GRCh38
NC_000004.11:g.6271094C= , CM000666.1:g.6271094C= GRCh37
NC_000004.10:g.6321995C= NCBI36
NG_011700.1:g.4518C=

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7728C= XP_016864075.1:n.4+7728C=