Canonical Allele Identifier: CA1435753429
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269463A= , CM000666.2:g.6269463A= GRCh38
NC_000004.11:g.6271190A= , CM000666.1:g.6271190A= GRCh37
NC_000004.10:g.6322091A= NCBI36
NG_011700.1:g.4614A=

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7824A= XP_016864075.1:n.4+7824A=