Canonical Allele Identifier: CA2034424974
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1592167147

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908790A>G , CM000674.2:g.47908790A>G GRCh38
NC_000012.11:g.48302573A>G , CM000674.1:g.48302573A>G GRCh37
NC_000012.10:g.46588840A>G NCBI36
NG_008731.1:g.1242T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-26016T>C ENSP00000378734.2:n.-83-26016T>C