LDH info

Canonical Allele Identifier: CA9273684
Gene: CYP4F2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 225969
dbSNP Id: rs2108622

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879621C>T , CM000681.2:g.15879621C>T GRCh38
NC_000019.9:g.15990431C>T , CM000681.1:g.15990431C>T GRCh37
NC_000019.8:g.15851431C>T NCBI36
NG_007971.2:g.23454G>A

Transcript Alleles

HGVS Amino-acid change
NM_001082.4:c.1297G>A VV NP_001073.3:p.Val433Met
NM_001082.5:c.1297G>A VV MANE Preferred NP_001073.3:p.Val433Met
ENST00000011989.11:c.1297G>A ENSP00000011989.8:p.Val433Met
ENST00000221700.10:c.1297G>A ENSP00000221700.3:p.Val433Met
ENST00000392846.7:n.1240G>A
ENST00000589654.2:n.103-193G>A