Canonical Allele Identifier: CA2795870183
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908701C>A , CM000674.2:g.47908701C>A GRCh38
NC_000012.11:g.48302484C>A , CM000674.1:g.48302484C>A GRCh37
NC_000012.10:g.46588751C>A NCBI36
NG_008731.1:g.1331G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-25927G>T ENSP00000378734.2:n.-83-25927G>T