Canonical Allele Identifier: CA2034424958
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908774T= , CM000674.2:g.47908774T= GRCh38
NC_000012.11:g.48302557T= , CM000674.1:g.48302557T= GRCh37
NC_000012.10:g.46588824T= NCBI36
NG_008731.1:g.1258A=

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-26000A= ENSP00000378734.2:n.-83-26000A=