Canonical Allele Identifier: CA797143858
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1352247433
MyVariant Identifiers: chr4:g.6271108T>A (hg19) chr4:g.6269381T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269381T>A , CM000666.2:g.6269381T>A GRCh38
NC_000004.11:g.6271108T>A , CM000666.1:g.6271108T>A GRCh37
NC_000004.10:g.6322009T>A NCBI36
NG_011700.1:g.4532T>A

Transcript Alleles

HGVS Amino-acid Change
XM_017008586.1:c.4+7742T>A XP_016864075.1:n.4+7742T>A
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