Canonical Allele Identifier: CA2034426873
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946710533

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910800A>G , CM000674.2:g.47910800A>G GRCh38
NC_000012.11:g.48304583A>G , CM000674.1:g.48304583A>G GRCh37
NC_000012.10:g.46590850A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-28026T>C ENSP00000378734.2:n.-83-28026T>C