Canonical Allele Identifier: CA1435753403
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs543039941

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269415A>G , CM000666.2:g.6269415A>G GRCh38
NC_000004.11:g.6271142A>G , CM000666.1:g.6271142A>G GRCh37
NC_000004.10:g.6322043A>G NCBI36
NG_011700.1:g.4566A>G

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7776A>G XP_016864075.1:n.4+7776A>G