LDH info

Canonical Allele Identifier: CA13646498
Gene: VDR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1544410

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47846052C>T , CM000674.2:g.47846052C>T GRCh38
NC_000012.11:g.48239835C>T , CM000674.1:g.48239835C>T GRCh37
NC_000012.10:g.46526102C>T NCBI36
NG_008731.1:g.63980G>A

Transcript Alleles

HGVS Amino-acid change
NM_000376.2:c.1024+283G>A VV NP_000367.1:p.=
NM_001017535.1:c.1024+283G>A VV NP_001017535.1:p.=
NM_001017536.1:c.1174+283G>A VV NP_001017536.1:p.=
XM_006719587.2:c.1024+283G>A XP_006719650.1:p.=
XM_011538720.1:c.1024+283G>A XP_011537022.1:p.=
NM_001364085.1:c.1024+283G>A VV NP_001351014.1:p.=
XM_006719587.3:c.1024+283G>A XP_006719650.1:p.=
XM_011538720.2:c.1024+283G>A XP_011537022.1:p.=
XM_024449178.1:c.1093+283G>A XP_024304946.1:p.=
NM_000376.3:c.1024+283G>A VV MANE Preferred NP_000367.1:p.=
NM_001017535.2:c.1024+283G>A VV NP_001017535.1:p.=
NM_001017536.2:c.1174+283G>A VV NP_001017536.1:p.=
NM_001364085.2:c.1024+283G>A VV NP_001351014.1:p.=
NM_001374661.1:c.1024+283G>A VV NP_001361590.1:p.=
NM_001374662.1:c.1024+283G>A VV NP_001361591.1:p.=
ENST00000229022.7:c.1024+283G>A ENSP00000229022.3:p.=
ENST00000395324.6:c.1024+283G>A ENSP00000378734.2:p.=
ENST00000547065.1:c.*1026+283G>A ENSP00000449074.1:p.=
ENST00000549336.5:c.1024+283G>A ENSP00000449573.1:p.=
ENST00000550325.5:c.1174+283G>A ENSP00000447173.1:p.=