Canonical Allele Identifier: CA947343884
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946697827

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908706C>T , CM000674.2:g.47908706C>T GRCh38
NC_000012.11:g.48302489C>T , CM000674.1:g.48302489C>T GRCh37
NC_000012.10:g.46588756C>T NCBI36
NG_008731.1:g.1326G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25932G>A ENSP00000378734.2:n.-83-25932G>A