Canonical Allele Identifier: CA236506083

Gene: VDR

Linked Data

• dbSNP Id: rs779388817
• MyVariant Identifiers: chr12:g.48302566A>G (hg19) ; chr12:g.47908783A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47908783A>G , CM000674.2:g.47908783A>G	GRCh38
NC_000012.11:g.48302566A>G , CM000674.1:g.48302566A>G	GRCh37
NC_000012.10:g.46588833A>G	NCBI36
NG_008731.1:g.1249T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395324.6:c.-83-26009T>C	ENSP00000378734.2:n.-83-26009T>C