LDH info

Canonical Allele Identifier: CA15969672
Gene: CSTF1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16979877

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.56392982A>G , CM000682.2:g.56392982A>G GRCh38
NC_000020.10:g.54968038A>G , CM000682.1:g.54968038A>G GRCh37
NC_000020.9:g.54401445A>G NCBI36
NG_012133.1:g.4314T>C

Transcript Alleles

HGVS Amino-acid change
NM_001033521.1:c.-33+444A>G VV NP_001028693.1:p.=
NM_001033522.1:c.-33+167A>G VV NP_001028694.1:p.=
NM_001324.2:c.-33+269A>G VV NP_001315.1:p.=
XM_011528600.1:c.-33+243A>G XP_011526902.1:p.=
ENST00000217109.8:c.-33+269A>G ENSP00000217109.4:p.=
ENST00000415828.5:c.-33+444A>G ENSP00000387968.1:p.=
ENST00000428552.1:c.-1+444A>G ENSP00000405171.1:p.=
ENST00000452950.1:c.-33+167A>G ENSP00000409035.1:p.=
ENST00000490539.1:c.-33+269A>G ENSP00000479273.1:p.=
ENST00000493039.5:c.-33+167A>G ENSP00000477958.1:p.=
ENST00000498689.5:n.168+444A>G
ENST00000613138.1:n.192+269A>G