Canonical Allele Identifier: CA2034424935
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946698021

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908750A>T , CM000674.2:g.47908750A>T GRCh38
NC_000012.11:g.48302533A>T , CM000674.1:g.48302533A>T GRCh37
NC_000012.10:g.46588800A>T NCBI36
NG_008731.1:g.1282T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25976T>A ENSP00000378734.2:n.-83-25976T>A