Canonical Allele Identifier: CA236507367
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs781645952
MyVariant Identifiers: chr12:g.48304610G>A (hg19) chr12:g.47910827G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910827G>A , CM000674.2:g.47910827G>A GRCh38
NC_000012.11:g.48304610G>A , CM000674.1:g.48304610G>A GRCh37
NC_000012.10:g.46590877G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-28053C>T ENSP00000378734.2:n.-83-28053C>T
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