Canonical Allele Identifier: CA2034426776
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946709868

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910680T>A , CM000674.2:g.47910680T>A GRCh38
NC_000012.11:g.48304463T>A , CM000674.1:g.48304463T>A GRCh37
NC_000012.10:g.46590730T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-27906A>T ENSP00000378734.2:n.-83-27906A>T