Canonical Allele Identifier: CA11634581
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs4320200
gnomAD v2: 4-6271043-A-T
gnomAD v3: 4-6269316-A-T
gnomAD v4: 4-6269316-A-T
MyVariant Identifiers: chr4:g.6271043A>T (hg19) chr4:g.6269316A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269316A>T , CM000666.2:g.6269316A>T GRCh38
NC_000004.11:g.6271043A>T , CM000666.1:g.6271043A>T GRCh37
NC_000004.10:g.6321944A>T NCBI36
NG_011700.1:g.4467A>T

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7677A>T XP_016864075.1:n.4+7677A>T
Search 100 bp 5'
Search 100 bp 3'