Canonical Allele Identifier: CA689466310
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1204229901
MyVariant Identifiers: chr12:g.48302456C>A (hg19) chr12:g.47908673C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908673C>A , CM000674.2:g.47908673C>A GRCh38
NC_000012.11:g.48302456C>A , CM000674.1:g.48302456C>A GRCh37
NC_000012.10:g.46588723C>A NCBI36
NG_008731.1:g.1359G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25899G>T ENSP00000378734.2:n.-83-25899G>T
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