Canonical Allele Identifier: CA2034424929
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908735C= , CM000674.2:g.47908735C= GRCh38
NC_000012.11:g.48302518C= , CM000674.1:g.48302518C= GRCh37
NC_000012.10:g.46588785C= NCBI36
NG_008731.1:g.1297G=

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25961G= ENSP00000378734.2:n.-83-25961G=