LDH info

Canonical Allele Identifier: CA273634
Gene: EMD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 179496
ClinVar RCV Id: RCV000156286
dbSNP Id: rs727504901

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379688A>G , CM000685.2:g.154379688A>G GRCh38
NC_000023.10:g.153608048A>G , CM000685.1:g.153608048A>G GRCh37
NC_000023.9:g.153261242A>G NCBI36
NG_008677.1:g.10253A>G , LRG_745:g.10253A>G

Transcript Alleles

HGVS Amino-acid change
NM_000117.2:c.83-2A>G , LRG_745t1:c.83-2A>G NP_000108.1:p.=
XM_024452349.1:c.-126-2A>G XP_024308117.1:p.=
NM_000117.3:c.83-2A>G VV MANE Preferred NP_000108.1:p.=
ENST00000369835.3:c.82+122A>G ENSP00000358850.3:p.=
ENST00000369842.8:c.83-2A>G ENSP00000358857.4:p.=
ENST00000428228.5:c.54-2A>G ENSP00000401081.1:p.=
ENST00000468294.5:n.43-2A>G
ENST00000485261.1:n.163+122A>G
ENST00000486738.5:n.227-2A>G
ENST00000492448.1:n.64A>G
ENST00000494443.5:n.140-2A>G