LDH info

Canonical Allele Identifier: CA122563
Gene: TF HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 12617
dbSNP Id: rs1049296

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133775510C>T , CM000665.2:g.133775510C>T GRCh38
NC_000003.11:g.133494354C>T , CM000665.1:g.133494354C>T GRCh37
NC_000003.10:g.134977044C>T NCBI36
NG_013080.1:g.34378C>T
NG_013080.2:g.118513C>T

Transcript Alleles

HGVS Amino-acid change
NM_001063.3:c.1765C>T VV NP_001054.1:p.Pro589Ser
XM_011513100.1:c.1765C>T XP_011511402.1:p.Pro589Ser
NM_001354703.1:c.1633C>T VV NP_001341632.1:p.Pro545Ser
NM_001354704.1:c.1384C>T VV NP_001341633.1:p.Pro462Ser
NM_001063.4:c.1765C>T VV MANE Preferred NP_001054.2:p.Pro589Ser
NM_001354703.2:c.1633C>T VV NP_001341632.2:p.Pro545Ser
NM_001354704.2:c.1384C>T VV NP_001341633.2:p.Pro462Ser
ENST00000402696.7:c.1765C>T ENSP00000385834.3:p.Pro589Ser
ENST00000461695.1:n.496C>T
ENST00000467842.1:n.2759C>T