LDH info

Canonical Allele Identifier: CA14440588
Gene: TRIM47 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1055129

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75876867A>G , CM000679.2:g.75876867A>G GRCh38
NC_000017.10:g.73872948A>G , CM000679.1:g.73872948A>G GRCh37
NC_000017.9:g.71384543A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_033452.2:c.676-54T>C VV NP_258411.2:p.=
XM_005257787.3:c.-39-54T>C XP_005257844.1:p.=
XM_005257788.3:c.-39-54T>C XP_005257845.1:p.=
XM_005257787.4:c.-39-54T>C XP_005257844.1:p.=
XM_005257788.5:c.-39-54T>C XP_005257845.1:p.=
NM_033452.3:c.676-54T>C VV MANE Preferred NP_258411.2:p.=
ENST00000254816.5:c.676-54T>C ENSP00000254816.1:p.=
ENST00000586495.1:c.-93T>C ENSP00000465038.1:p.=
ENST00000587339.2:n.347-54T>C
ENST00000587774.1:n.341-54T>C