Canonical Allele Identifier: CA2795870239
Gene: VDR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910782G>T , CM000674.2:g.47910782G>T GRCh38
NC_000012.11:g.48304565G>T , CM000674.1:g.48304565G>T GRCh37
NC_000012.10:g.46590832G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-28008C>A ENSP00000378734.2:n.-83-28008C>A
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