Canonical Allele Identifier: CA11677666
Gene: WFS1 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.6269689G>T
GRCh37 chr4:g.6271416G>T
gnomAD v2:
4:6271416 G / T
gnomAD v3:
4:6269689 G / T
gnomAD v4:
chr4-6269689-G-T
Joint Max Group AF 0.91060865 (EAS)
Genomes Max Group AF 0.91060865 (EAS)
ClinVar RCV:
RCV000844553
ClinVar Variation:
684340
dbSNP:
4273545
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269689G>T , CM000666.2:g.6269689G>T GRCh38
NC_000004.11:g.6271416G>T , CM000666.1:g.6271416G>T GRCh37
NC_000004.10:g.6322317G>T NCBI36
NG_011700.1:g.4840G>T

Transcript Alleles

HGVS Amino-acid Change
XM_017008586.1:c.5-7762G>T XP_016864075.1:n.5-7762G>T
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