LDH info

Canonical Allele Identifier: CA121389
Gene: EMD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11179
ClinVar RCV Id: RCV000011929
dbSNP Id: rs104894806

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380979C>A , CM000685.2:g.154380979C>A GRCh38
NC_000023.10:g.153609339C>A , CM000685.1:g.153609339C>A GRCh37
NC_000023.9:g.153262533C>A NCBI36
NG_008677.1:g.11544C>A , LRG_745:g.11544C>A

Transcript Alleles

HGVS Amino-acid change
NM_000117.2:c.547C>A , LRG_745t1:c.547C>A NP_000108.1:p.Pro183Thr
XM_024452349.1:c.553C>A XP_024308117.1:p.Pro185Thr
NM_000117.3:c.547C>A VV MANE Preferred NP_000108.1:p.Pro183Thr
ENST00000369835.3:c.442C>A ENSP00000358850.3:p.Pro148Thr
ENST00000369842.8:c.547C>A ENSP00000358857.4:p.Pro183Thr
ENST00000428228.5:c.*452C>A ENSP00000401081.1:p.=
ENST00000471965.1:n.336C>A
ENST00000486738.5:n.984C>A
ENST00000492448.1:n.530C>A