Canonical Allele Identifier: CA2034422773
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47906043T= , CM000674.2:g.47906043T= GRCh38
NC_000012.11:g.48299826T= , CM000674.1:g.48299826T= GRCh37
NC_000012.10:g.46586093T= NCBI36
NG_008731.1:g.3989A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395324.6:c.-83-23269A= ENSP00000378734.2:n.-83-23269A=