LDH info

Canonical Allele Identifier: CA322803381
Gene: MYO18B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1001021

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26007633G>A , CM000684.2:g.26007633G>A GRCh38
NC_000022.10:g.26403599G>A , CM000684.1:g.26403599G>A GRCh37
NC_000022.9:g.24733599G>A NCBI36
NG_046772.1:g.270490G>A

Transcript Alleles

HGVS Amino-acid change
NM_032608.5:c.6470+2778G>A VV NP_115997.5:p.=
XM_005261786.3:c.6473+2778G>A XP_005261843.1:p.=
XM_011530458.1:c.6599+2778G>A XP_011528760.1:p.=
XM_011530459.1:c.6599+2778G>A XP_011528761.1:p.=
XM_011530460.1:c.6599+2778G>A XP_011528762.1:p.=
XM_011530461.1:c.6599+2778G>A XP_011528763.1:p.=
XM_011530462.1:c.6599+2778G>A XP_011528764.1:p.=
XM_011530463.1:c.6599+2778G>A XP_011528765.1:p.=
XM_011530464.1:c.6596+2778G>A XP_011528766.1:p.=
XM_011530465.1:c.6116+2778G>A XP_011528767.1:p.=
NM_001318245.1:c.6473+2778G>A VV NP_001305174.1:p.=
NM_032608.6:c.6470+2778G>A VV NP_115997.5:p.=
XM_011530458.2:c.6599+2778G>A XP_011528760.1:p.=
XM_011530459.2:c.6599+2778G>A XP_011528761.1:p.=
XM_011530460.2:c.6599+2778G>A XP_011528762.1:p.=
XM_011530461.2:c.6599+2778G>A XP_011528763.1:p.=
XM_011530464.2:c.6596+2778G>A XP_011528766.1:p.=
XM_011530465.2:c.6116+2778G>A XP_011528767.1:p.=
XM_017029012.1:c.6599+2778G>A XP_016884501.1:p.=
XM_017029013.1:c.6599+2778G>A XP_016884502.1:p.=
XM_017029014.1:c.6596+2778G>A XP_016884503.1:p.=
XM_017029015.1:c.6467+2778G>A XP_016884504.1:p.=
XM_017029016.1:c.3935+2778G>A XP_016884505.1:p.=
XM_017029017.1:c.3932+2778G>A XP_016884506.1:p.=
NM_001318245.2:c.6473+2778G>A VV NP_001305174.1:p.=
NM_032608.7:c.6470+2778G>A VV MANE Preferred NP_115997.5:p.=
ENST00000335473.11:c.6470+2778G>A ENSP00000334563.7:p.=
ENST00000407587.6:c.6473+2778G>A ENSP00000386096.2:p.=
ENST00000418374.6:n.5041+2778G>A
ENST00000536101.5:c.6470+2778G>A ENSP00000441229.1:p.=
ENST00000539302.5:c.*3928+2778G>A ENSP00000437587.1:p.=
ENST00000543971.1:n.319+2778G>A