LDH info

Canonical Allele Identifier: CA119592
Gene: CYP2C9 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 8409
dbSNP Id: rs1799853

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942290C>T , CM000672.2:g.94942290C>T GRCh38
NC_000010.10:g.96702047C>T , CM000672.1:g.96702047C>T GRCh37
NC_000010.9:g.96692037C>T NCBI36
NG_008385.1:g.8633C>T
NG_008385.2:g.9133C>T

Transcript Alleles

HGVS Amino-acid change
NM_000771.3:c.430C>T VV NP_000762.2:p.Arg144Cys
NM_000771.4:c.430C>T VV NP_000762.2:p.Arg144Cys
ENST00000260682.6:c.430C>T ENSP00000260682.6:p.Arg144Cys
ENST00000461906.1:n.455C>T
ENST00000473496.1:n.201C>T