Canonical Allele Identifier: CA689466866

Gene: VDR

Linked Data

• dbSNP Id: rs1236994277
• gnomAD v3: 12-47856079-A-C
• gnomAD v4: 12-47856079-A-C
• MyVariant Identifiers: chr12:g.48249862A>C (hg19) ; chr12:g.47856079A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47856079A>C , CM000674.2:g.47856079A>C	GRCh38
NC_000012.11:g.48249862A>C , CM000674.1:g.48249862A>C	GRCh37
NC_000012.10:g.46536129A>C	NCBI36
NG_008731.1:g.53953T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229022.9:c.584-278T>G	ENSP00000229022.5:n.584-278T>G
ENST00000549336.6:c.584-278T>G MANE Select	ENSP00000449573.2:n.584-278T>G
ENST00000229022.7:c.584-278T>G	ENSP00000229022.3:n.584-278T>G
ENST00000395324.6:c.584-278T>G	ENSP00000378734.2:n.584-278T>G
ENST00000546653.5:c.584-278T>G	ENSP00000448659.1:n.584-278T>G
ENST00000547065.1:c.*586-278T>G	ENSP00000449074.1:n.*586-278T>G
ENST00000549336.5:c.584-278T>G	ENSP00000449573.1:n.584-278T>G
ENST00000550325.5:c.734-278T>G	ENSP00000447173.1:n.734-278T>G
NM_000376.2:c.584-278T>G	NP_000367.1:n.584-278T>G
NM_001017535.1:c.584-278T>G	NP_001017535.1:n.584-278T>G
NM_001017536.1:c.734-278T>G	NP_001017536.1:n.734-278T>G
XM_006719587.2:c.584-278T>G	XP_006719650.1:n.584-278T>G
XM_011538720.1:c.584-278T>G	XP_011537022.1:n.584-278T>G
NM_001364085.1:c.584-278T>G	NP_001351014.1:n.584-278T>G
XM_006719587.3:c.584-278T>G	XP_006719650.1:n.584-278T>G
XM_011538720.2:c.584-278T>G	XP_011537022.1:n.584-278T>G
XM_024449178.1:c.653-278T>G	XP_024304946.1:n.653-278T>G
NM_000376.3:c.584-278T>G MANE Select	NP_000367.1:n.584-278T>G
NM_001017535.2:c.584-278T>G	NP_001017535.1:n.584-278T>G
NM_001017536.2:c.734-278T>G	NP_001017536.1:n.734-278T>G
NM_001364085.2:c.584-278T>G	NP_001351014.1:n.584-278T>G
NM_001374661.1:c.584-278T>G	NP_001361590.1:n.584-278T>G
NM_001374662.1:c.584-278T>G	NP_001361591.1:n.584-278T>G