Canonical Allele Identifier: CA689466309
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1484054765
MyVariant Identifiers: chr12:g.48302453A>C (hg19) chr12:g.47908670A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908670A>C , CM000674.2:g.47908670A>C GRCh38
NC_000012.11:g.48302453A>C , CM000674.1:g.48302453A>C GRCh37
NC_000012.10:g.46588720A>C NCBI36
NG_008731.1:g.1362T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25896T>G ENSP00000378734.2:n.-83-25896T>G
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