Canonical Allele Identifier: CA236506025
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs779958864
MyVariant Identifiers: chr12:g.48302458G>A (hg19) chr12:g.47908675G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908675G>A , CM000674.2:g.47908675G>A GRCh38
NC_000012.11:g.48302458G>A , CM000674.1:g.48302458G>A GRCh37
NC_000012.10:g.46588725G>A NCBI36
NG_008731.1:g.1357C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25901C>T ENSP00000378734.2:n.-83-25901C>T
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