Canonical Allele Identifier: CA604844578
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1472990524
gnomAD v2: 12-48302560-C-T
gnomAD v3: 12-47908777-C-T
gnomAD v4: 12-47908777-C-T
MyVariant Identifiers: chr12:g.48302560C>T (hg19) chr12:g.47908777C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908777C>T , CM000674.2:g.47908777C>T GRCh38
NC_000012.11:g.48302560C>T , CM000674.1:g.48302560C>T GRCh37
NC_000012.10:g.46588827C>T NCBI36
NG_008731.1:g.1255G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-26003G>A ENSP00000378734.2:n.-83-26003G>A
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