Canonical Allele Identifier: CA236506060
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs958096891
MyVariant Identifiers: chr12:g.48302517G>T (hg19) chr12:g.47908734G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908734G>T , CM000674.2:g.47908734G>T GRCh38
NC_000012.11:g.48302517G>T , CM000674.1:g.48302517G>T GRCh37
NC_000012.10:g.46588784G>T NCBI36
NG_008731.1:g.1298C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25960C>A ENSP00000378734.2:n.-83-25960C>A
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