Canonical Allele Identifier: CA2034424891
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946697689

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908664T>C , CM000674.2:g.47908664T>C GRCh38
NC_000012.11:g.48302447T>C , CM000674.1:g.48302447T>C GRCh37
NC_000012.10:g.46588714T>C NCBI36
NG_008731.1:g.1368A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25890A>G ENSP00000378734.2:n.-83-25890A>G