Canonical Allele Identifier: CA91777153
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs964439344
MyVariant Identifiers: chr4:g.6269431G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269431G>T , CM000666.2:g.6269431G>T GRCh38
NC_000004.11:g.6271158G>T , CM000666.1:g.6271158G>T GRCh37
NC_000004.10:g.6322059G>T NCBI36
NG_011700.1:g.4582G>T

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7792G>T XP_016864075.1:n.4+7792G>T