LDH info

Canonical Allele Identifier: CA019631
Gene: ACTC1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 18324
ClinVar RCV Id: RCV000019989
dbSNP Id: rs121912674

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34790458T>C , CM000677.2:g.34790458T>C GRCh38
NC_000015.9:g.35082659T>C , CM000677.1:g.35082659T>C GRCh37
NC_000015.8:g.32869951T>C NCBI36
NG_007553.1:g.10269A>G , LRG_388:g.10269A>G

Transcript Alleles

HGVS Amino-acid change
NM_005159.4:c.1088A>G , LRG_388t1:c.1088A>G NP_005150.1:p.Glu363Gly
NR_120329.1:n.299+13027T>C
NM_005159.5:c.1088A>G VV MANE Preferred NP_005150.1:p.Glu363Gly
ENST00000290378.4:c.1088A>G ENSP00000290378.4:p.Glu363Gly