Canonical Allele Identifier: CA91777006

Gene: WFS1

Linked Data

• dbSNP Id: rs1018814462
• gnomAD v2: 4-6271057-T-A
• gnomAD v3: 4-6269330-T-A
• gnomAD v4: 4-6269330-T-A
• MyVariant Identifiers: chr4:g.6271057T>A (hg19) ; chr4:g.6269330T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6269330T>A , CM000666.2:g.6269330T>A	GRCh38
NC_000004.11:g.6271057T>A , CM000666.1:g.6271057T>A	GRCh37
NC_000004.10:g.6321958T>A	NCBI36
NG_011700.1:g.4481T>A

Transcript Alleles

HGVS	Amino-acid change
XM_017008586.1:c.4+7691T>A	XP_016864075.1:n.4+7691T>A