Canonical Allele Identifier: CA689467461

Gene: VDR

Linked Data

• dbSNP Id: rs1464124801
• MyVariant Identifiers: chr12:g.48304558C>G (hg19) ; chr12:g.47910775C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47910775C>G , CM000674.2:g.47910775C>G	GRCh38
NC_000012.11:g.48304558C>G , CM000674.1:g.48304558C>G	GRCh37
NC_000012.10:g.46590825C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395324.6:c.-83-28001G>C	ENSP00000378734.2:n.-83-28001G>C