Canonical Allele Identifier: CA2034426892
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1199219769
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910812C>T , CM000674.2:g.47910812C>T GRCh38
NC_000012.11:g.48304595C>T , CM000674.1:g.48304595C>T GRCh37
NC_000012.10:g.46590862C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-28038G>A ENSP00000378734.2:n.-83-28038G>A
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