Canonical Allele Identifier: CA2705215163
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs2109102572

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269438A>G , CM000666.2:g.6269438A>G GRCh38
NC_000004.11:g.6271165A>G , CM000666.1:g.6271165A>G GRCh37
NC_000004.10:g.6322066A>G NCBI36
NG_011700.1:g.4589A>G

Transcript Alleles

HGVS Amino-acid Change
XM_017008586.1:c.4+7799A>G XP_016864075.1:n.4+7799A>G