Canonical Allele Identifier: CA2034426885
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1168217859

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910810C>A , CM000674.2:g.47910810C>A GRCh38
NC_000012.11:g.48304593C>A , CM000674.1:g.48304593C>A GRCh37
NC_000012.10:g.46590860C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-28036G>T ENSP00000378734.2:n.-83-28036G>T