Canonical Allele Identifier: CA2034424902
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946697768
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908678G>A , CM000674.2:g.47908678G>A GRCh38
NC_000012.11:g.48302461G>A , CM000674.1:g.48302461G>A GRCh37
NC_000012.10:g.46588728G>A NCBI36
NG_008731.1:g.1354C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25904C>T ENSP00000378734.2:n.-83-25904C>T
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