Canonical Allele Identifier: CA2034424983
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908807A= , CM000674.2:g.47908807A= GRCh38
NC_000012.11:g.48302590A= , CM000674.1:g.48302590A= GRCh37
NC_000012.10:g.46588857A= NCBI36
NG_008731.1:g.1225T=

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-26033T= ENSP00000378734.2:n.-83-26033T=