LDH info

Canonical Allele Identifier: CA261238
Gene: PYGM HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 40042
ClinVar RCV Id: RCV000033140
dbSNP Id: rs397514631

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759747T>C , CM000673.2:g.64759747T>C GRCh38
NC_000011.9:g.64527219T>C , CM000673.1:g.64527219T>C GRCh37
NC_000011.8:g.64283795T>C NCBI36
NG_013018.1:g.5969A>G

Transcript Alleles

HGVS Amino-acid change
NM_001164716.1:c.152A>G VV NP_001158188.1:p.Asp51Gly
NM_005609.2:c.152A>G VV NP_005600.1:p.Asp51Gly
NM_005609.3:c.152A>G VV NP_005600.1:p.Asp51Gly
NM_005609.4:c.152A>G VV MANE Preferred NP_005600.1:p.Asp51Gly
ENST00000164139.3:c.152A>G ENSP00000164139.3:p.Asp51Gly
ENST00000377432.7:c.152A>G ENSP00000366650.3:p.Asp51Gly