Canonical Allele Identifier: CA689466339
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1265368261
MyVariant Identifiers: chr12:g.48302518C>A (hg19) chr12:g.47908735C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908735C>A , CM000674.2:g.47908735C>A GRCh38
NC_000012.11:g.48302518C>A , CM000674.1:g.48302518C>A GRCh37
NC_000012.10:g.46588785C>A NCBI36
NG_008731.1:g.1297G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25961G>T ENSP00000378734.2:n.-83-25961G>T
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