Canonical Allele Identifier: CA1435753363
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1729727784

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269349C>G , CM000666.2:g.6269349C>G GRCh38
NC_000004.11:g.6271076C>G , CM000666.1:g.6271076C>G GRCh37
NC_000004.10:g.6321977C>G NCBI36
NG_011700.1:g.4500C>G

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7710C>G XP_016864075.1:n.4+7710C>G