Canonical Allele Identifier: CA947343882
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs1946697675

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47908663A>T , CM000674.2:g.47908663A>T GRCh38
NC_000012.11:g.48302446A>T , CM000674.1:g.48302446A>T GRCh37
NC_000012.10:g.46588713A>T NCBI36
NG_008731.1:g.1369T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395324.6:c.-83-25889T>A ENSP00000378734.2:n.-83-25889T>A