Canonical Allele Identifier: CA236507361

Gene: VDR

Linked Data

• dbSNP Id: rs766513913
• MyVariant Identifiers: chr12:g.48304591T>G (hg19) ; chr12:g.47910808T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47910808T>G , CM000674.2:g.47910808T>G	GRCh38
NC_000012.11:g.48304591T>G , CM000674.1:g.48304591T>G	GRCh37
NC_000012.10:g.46590858T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395324.6:c.-83-28034A>C	ENSP00000378734.2:n.-83-28034A>C