Canonical Allele Identifier: CA2034424952
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946698217

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908768C>T , CM000674.2:g.47908768C>T GRCh38
NC_000012.11:g.48302551C>T , CM000674.1:g.48302551C>T GRCh37
NC_000012.10:g.46588818C>T NCBI36
NG_008731.1:g.1264G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25994G>A ENSP00000378734.2:n.-83-25994G>A