Canonical Allele Identifier: CA2034424968
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946698352

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908787T>C , CM000674.2:g.47908787T>C GRCh38
NC_000012.11:g.48302570T>C , CM000674.1:g.48302570T>C GRCh37
NC_000012.10:g.46588837T>C NCBI36
NG_008731.1:g.1245A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-26013A>G ENSP00000378734.2:n.-83-26013A>G