Canonical Allele Identifier: CA91776998
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs572058489
gnomAD v2: 4-6271041-G-A
gnomAD v3: 4-6269314-G-A
gnomAD v4: 4-6269314-G-A
MyVariant Identifiers: chr4:g.6271041G>A (hg19) chr4:g.6269314G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269314G>A , CM000666.2:g.6269314G>A GRCh38
NC_000004.11:g.6271041G>A , CM000666.1:g.6271041G>A GRCh37
NC_000004.10:g.6321942G>A NCBI36
NG_011700.1:g.4465G>A

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7675G>A XP_016864075.1:n.4+7675G>A
Search 100 bp 5'
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