Canonical Allele Identifier: CA2034426780
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47910694A= , CM000674.2:g.47910694A= GRCh38
NC_000012.11:g.48304477A= , CM000674.1:g.48304477A= GRCh37
NC_000012.10:g.46590744A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-27920T= ENSP00000378734.2:n.-83-27920T=