Canonical Allele Identifier: CA2034426860
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946710420
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910783G>A , CM000674.2:g.47910783G>A GRCh38
NC_000012.11:g.48304566G>A , CM000674.1:g.48304566G>A GRCh37
NC_000012.10:g.46590833G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-28009C>T ENSP00000378734.2:n.-83-28009C>T
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