LDH info

Canonical Allele Identifier: CA116353
Gene: ABCC11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 3558
dbSNP Id: rs17822931

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.48224287C>T , CM000678.2:g.48224287C>T GRCh38
NC_000016.9:g.48258198C>T , CM000678.1:g.48258198C>T GRCh37
NC_000016.8:g.46815699C>T NCBI36
NG_011522.1:g.15891G>A

Transcript Alleles

HGVS Amino-acid change
NM_032583.3:c.538G>A VV NP_115972.2:p.Gly180Arg
NM_033151.3:c.538G>A VV NP_149163.2:p.Gly180Arg
NM_145186.2:c.538G>A VV NP_660187.1:p.Gly180Arg
XM_011523396.1:c.340G>A XP_011521698.1:p.Gly114Arg
XM_017023795.2:c.538G>A XP_016879284.1:p.Gly180Arg
XM_017023796.2:c.538G>A XP_016879285.1:p.Gly180Arg
XM_017023797.2:c.538G>A XP_016879286.1:p.Gly180Arg
XM_017023798.2:c.538G>A XP_016879287.1:p.Gly180Arg
XM_017023799.2:c.538G>A XP_016879288.1:p.Gly180Arg
XM_017023800.2:c.538G>A XP_016879289.1:p.Gly180Arg
XM_017023801.2:c.538G>A XP_016879290.1:p.Gly180Arg
XM_017023803.1:c.538G>A XP_016879292.1:p.Gly180Arg
XR_001752012.1:n.3216G>A
ENST00000353782.9:c.538G>A ENSP00000311326.6:p.Gly180Arg
ENST00000356608.6:c.538G>A ENSP00000349017.2:p.Gly180Arg
ENST00000394747.5:c.538G>A ENSP00000378230.1:p.Gly180Arg
ENST00000394748.5:c.538G>A ENSP00000378231.1:p.Gly180Arg
ENST00000567385.5:n.936G>A