Canonical Allele Identifier: CA2034426778
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910686G= , CM000674.2:g.47910686G= GRCh38
NC_000012.11:g.48304469G= , CM000674.1:g.48304469G= GRCh37
NC_000012.10:g.46590736G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-27912C= ENSP00000378734.2:n.-83-27912C=