Canonical Allele Identifier: CA13646528
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs7976091

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910769C>T , CM000674.2:g.47910769C>T GRCh38
NC_000012.11:g.48304552C>T , CM000674.1:g.48304552C>T GRCh37
NC_000012.10:g.46590819C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-27995G>A ENSP00000378734.2:n.-83-27995G>A