Canonical Allele Identifier: CA91777057
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs957107701
gnomAD v3: 4-6269351-G-A
gnomAD v4: 4-6269351-G-A
MyVariant Identifiers: chr4:g.6271078G>A (hg19) chr4:g.6269351G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269351G>A , CM000666.2:g.6269351G>A GRCh38
NC_000004.11:g.6271078G>A , CM000666.1:g.6271078G>A GRCh37
NC_000004.10:g.6321979G>A NCBI36
NG_011700.1:g.4502G>A

Transcript Alleles

HGVS Amino-acid Change
XM_017008586.1:c.4+7712G>A XP_016864075.1:n.4+7712G>A
Search 100 bp 5'
Search 100 bp 3'