Canonical Allele Identifier: CA2618489023
Gene: VDR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47905035C>A , CM000674.2:g.47905035C>A GRCh38
NC_000012.11:g.48298818C>A , CM000674.1:g.48298818C>A GRCh37
NC_000012.10:g.46585085C>A NCBI36
NG_008731.1:g.4997G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-22261G>T ENSP00000378734.2:n.-83-22261G>T
ENST00000548664.1:c.-286G>T ENSP00000450105.1:n.-286G>T