Canonical Allele Identifier: CA2034426829
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946710180

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910747G>T , CM000674.2:g.47910747G>T GRCh38
NC_000012.11:g.48304530G>T , CM000674.1:g.48304530G>T GRCh37
NC_000012.10:g.46590797G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-27973C>A ENSP00000378734.2:n.-83-27973C>A