Canonical Allele Identifier: CA15761659
Gene: VDR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2239181

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47862166A>C , CM000674.2:g.47862166A>C GRCh38
NC_000012.11:g.48255949A>C , CM000674.1:g.48255949A>C GRCh37
NC_000012.10:g.46542216A>C NCBI36
NG_008731.1:g.47866T>G

Transcript Alleles

HGVS Amino-acid change
NM_000376.2:c.277+2881T>G VV NP_000367.1:p.=
NM_001017535.1:c.277+2881T>G VV NP_001017535.1:p.=
NM_001017536.1:c.427+2881T>G VV NP_001017536.1:p.=
XM_006719587.2:c.277+2881T>G XP_006719650.1:p.=
XM_011538720.1:c.277+2881T>G XP_011537022.1:p.=
NM_001364085.1:c.277+2881T>G VV NP_001351014.1:p.=
XM_006719587.3:c.277+2881T>G
XM_011538720.2:c.277+2881T>G
XM_024449178.1:c.346+2881T>G XP_024304946.1:p.=
ENST00000229022.7:c.277+2881T>G ENSP00000229022.3:p.=
ENST00000395324.6:c.277+2881T>G ENSP00000378734.2:p.=
ENST00000546653.5:c.277+2881T>G ENSP00000448659.1:p.=
ENST00000547065.1:c.*279+2881T>G ENSP00000449074.1:p.=
ENST00000548664.1:c.277+2881T>G ENSP00000450105.1:p.=
ENST00000549336.5:c.277+2881T>G ENSP00000449573.1:p.=
ENST00000550314.5:c.277+2881T>G ENSP00000449561.1:p.=
ENST00000550325.5:c.427+2881T>G ENSP00000447173.1:p.=