Canonical Allele Identifier: CA689467442

Gene: VDR

Linked Data

• dbSNP Id: rs1038519801
• MyVariant Identifiers: chr12:g.48304535C>T (hg19) ; chr12:g.47910752C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47910752C>T , CM000674.2:g.47910752C>T	GRCh38
NC_000012.11:g.48304535C>T , CM000674.1:g.48304535C>T	GRCh37
NC_000012.10:g.46590802C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395324.6:c.-83-27978G>A	ENSP00000378734.2:n.-83-27978G>A