Canonical Allele Identifier: CA549420840
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1302929363
gnomAD v2: 4-6271200-G-C
gnomAD v3: 4-6269473-G-C
gnomAD v4: 4-6269473-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269473G>C , CM000666.2:g.6269473G>C GRCh38
NC_000004.11:g.6271200G>C , CM000666.1:g.6271200G>C GRCh37
NC_000004.10:g.6322101G>C NCBI36
NG_011700.1:g.4624G>C

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7834G>C XP_016864075.1:n.4+7834G>C