Canonical Allele Identifier: CA2838022220
Gene: VDR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910769C>A , CM000674.2:g.47910769C>A GRCh38
NC_000012.11:g.48304552C>A , CM000674.1:g.48304552C>A GRCh37
NC_000012.10:g.46590819C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-27995G>T ENSP00000378734.2:n.-83-27995G>T
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