Canonical Allele Identifier: CA689466370
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1370911890
gnomAD v3: 12-47908799-T-C
gnomAD v4: 12-47908799-T-C
MyVariant Identifiers: chr12:g.48302582T>C (hg19) chr12:g.47908799T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908799T>C , CM000674.2:g.47908799T>C GRCh38
NC_000012.11:g.48302582T>C , CM000674.1:g.48302582T>C GRCh37
NC_000012.10:g.46588849T>C NCBI36
NG_008731.1:g.1233A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-26025A>G ENSP00000378734.2:n.-83-26025A>G
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