LDH info

Canonical Allele Identifier: CA339924
Gene: LRRK2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1939
ClinVar RCV Id: RCV000002016
dbSNP Id: rs34805604

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40299125A>G , CM000674.2:g.40299125A>G GRCh38
NC_000012.11:g.40692927A>G , CM000674.1:g.40692927A>G GRCh37
NC_000012.10:g.38979194A>G NCBI36
NG_011709.1:g.79115A>G

Transcript Alleles

HGVS Amino-acid change
NM_198578.3:c.3364A>G VV NP_940980.3:p.Ile1122Val
XM_005268629.2:c.3364A>G XP_005268686.1:p.Ile1122Val
XM_011537877.1:c.3364A>G XP_011536179.1:p.Ile1122Val
XM_011537878.1:c.3364A>G XP_011536180.1:p.Ile1122Val
XM_011537879.1:c.2161A>G XP_011536181.1:p.Ile721Val
XM_011537880.1:c.3364A>G XP_011536182.1:p.Ile1122Val
XM_011537881.1:c.3364A>G XP_011536183.1:p.Ile1122Val
XM_011537882.1:c.3364A>G XP_011536184.1:p.Ile1122Val
XM_005268629.4:c.3364A>G XP_005268686.1:p.Ile1122Val
XM_011537877.3:c.3364A>G XP_011536179.1:p.Ile1122Val
XM_011537881.3:c.3364A>G XP_011536183.1:p.Ile1122Val
XM_011537882.3:c.3364A>G XP_011536184.1:p.Ile1122Val
XM_017018786.2:c.3364A>G XP_016874275.1:p.Ile1122Val
XM_017018787.1:c.280A>G XP_016874276.1:p.Ile94Val
XM_017018789.2:c.3364A>G XP_016874278.1:p.Ile1122Val
XM_024448833.1:c.2161A>G XP_024304601.1:p.Ile721Val
XR_001748574.2:n.3606A>G
NM_198578.4:c.3364A>G VV MANE Preferred NP_940980.4:p.Ile1122Val
ENST00000298910.11:c.3364A>G ENSP00000298910.7:p.Ile1122Val
ENST00000343742.6:c.3364A>G ENSP00000341930.2:p.Ile1122Val
ENST00000430804.5:n.408A>G
ENST00000479187.5:n.45A>G