LDH info

Canonical Allele Identifier: CA4565829
Gene: AOC1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10156191

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150856517C>T , CM000669.2:g.150856517C>T GRCh38
NC_000007.13:g.150553605C>T , CM000669.1:g.150553605C>T GRCh37
NC_000007.12:g.150184538C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001091.3:c.47C>T VV NP_001082.2:p.Thr16Met
NM_001272072.1:c.47C>T VV NP_001259001.1:p.Thr16Met
XM_011516008.1:c.47C>T XP_011514310.1:p.Thr16Met
XM_011516009.1:c.47C>T XP_011514311.1:p.Thr16Met
XR_928169.1:n.296-15072G>A
XR_928170.1:n.425+12099G>A
XR_928171.1:n.298-15072G>A
XM_017011944.1:c.47C>T XP_016867433.1:p.Thr16Met
XM_017011945.1:c.47C>T XP_016867434.1:p.Thr16Met
XM_017011946.2:c.47C>T XP_016867435.1:p.Thr16Met
XM_017011947.1:c.47C>T XP_016867436.1:p.Thr16Met
XR_928169.2:n.302-15072G>A
XR_928171.2:n.302-15072G>A
NM_001091.4:c.47C>T VV NP_001082.2:p.Thr16Met
NM_001272072.2:c.47C>T VV NP_001259001.1:p.Thr16Met
ENST00000360937.8:c.47C>T ENSP00000354193.4:p.Thr16Met
ENST00000416793.6:c.47C>T ENSP00000411613.2:p.Thr16Met
ENST00000460213.1:c.47C>T ENSP00000418557.1:p.Thr16Met
ENST00000467291.5:c.47C>T ENSP00000418328.1:p.Thr16Met
ENST00000483043.1:c.47C>T ENSP00000417392.1:p.Thr16Met
ENST00000493429.5:c.47C>T ENSP00000418614.1:p.Thr16Met
ENST00000619575.1:c.47C>T ENSP00000481717.1:p.Thr16Met
ENST00000622116.4:c.-1376C>T ENSP00000481520.1:p.=