Canonical Allele Identifier: CA2618489036
Gene: VDR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47905042G>T , CM000674.2:g.47905042G>T GRCh38
NC_000012.11:g.48298825G>T , CM000674.1:g.48298825G>T GRCh37
NC_000012.10:g.46585092G>T NCBI36
NG_008731.1:g.4990C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-22268C>A ENSP00000378734.2:n.-83-22268C>A