Canonical Allele Identifier: CA2034424922
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908729T= , CM000674.2:g.47908729T= GRCh38
NC_000012.11:g.48302512T= , CM000674.1:g.48302512T= GRCh37
NC_000012.10:g.46588779T= NCBI36
NG_008731.1:g.1303A=

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25955A= ENSP00000378734.2:n.-83-25955A=