LDH info

Canonical Allele Identifier: CA250025
Gene: COQ2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1440
dbSNP Id: rs121918233

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.83279081C>T , CM000666.2:g.83279081C>T GRCh38
NC_000004.11:g.84200234C>T , CM000666.1:g.84200234C>T GRCh37
NC_000004.10:g.84419258C>T NCBI36
NG_015825.1:g.10834G>A

Transcript Alleles

HGVS Amino-acid change
NM_015697.7:n.437G>A VV NP_056512.5:p.Ser146Asn
XM_011531855.1:c.437G>A XP_011530157.1:p.Ser146Asn
XM_011531856.1:c.437G>A XP_011530158.1:p.Ser146Asn
XM_011531857.1:c.437G>A XP_011530159.1:p.Ser146Asn
XM_011531858.1:c.437G>A XP_011530160.1:p.Ser146Asn
XM_011531859.1:c.437G>A XP_011530161.1:p.Ser146Asn
XM_011531860.1:c.437G>A XP_011530162.1:p.Ser146Asn
XM_011531861.1:c.437G>A XP_011530163.1:p.Ser146Asn
XM_011531862.1:c.437G>A XP_011530164.1:p.Ser146Asn
XM_011531863.1:c.437G>A XP_011530165.1:p.Ser146Asn
XM_011531864.1:c.437G>A XP_011530166.1:p.Ser146Asn
XM_011531865.1:c.437G>A XP_011530167.1:p.Ser146Asn
XM_011531866.1:c.437G>A XP_011530168.1:p.Ser146Asn
XM_011531867.1:c.83G>A XP_011530169.1:p.Ser28Asn
XR_427543.2:n.596G>A
XR_938721.1:n.612G>A
NM_001358921.1:c.287G>A VV NP_001345850.1:p.Ser96Asn
NM_015697.8:c.437G>A VV NP_056512.5:p.Ser146Asn
XM_011531855.3:c.287G>A XP_011530157.2:p.Ser96Asn
XM_011531857.3:c.287G>A XP_011530159.2:p.Ser96Asn
XM_011531859.3:c.287G>A XP_011530161.2:p.Ser96Asn
XM_011531860.3:c.287G>A XP_011530162.2:p.Ser96Asn
XM_011531862.3:c.287G>A XP_011530164.2:p.Ser96Asn
XM_011531863.3:c.287G>A XP_011530165.2:p.Ser96Asn
XM_011531866.3:c.287G>A XP_011530168.2:p.Ser96Asn
XM_011531867.3:c.83G>A XP_011530169.1:p.Ser28Asn
XM_017008031.2:c.83G>A XP_016863520.1:p.Ser28Asn
XR_001741203.2:n.318G>A
XR_001741204.2:n.318G>A
XR_427543.4:n.318G>A
XR_938721.3:n.318G>A
ENST00000311461.7:c.287G>A ENSP00000311835.7:p.Ser96Asn
ENST00000311469.8:n.437G>A ENSP00000310873.4:p.Ser146Asn
ENST00000503391.5:c.287G>A ENSP00000426242.1:p.Ser96Asn
ENST00000514935.1:n.199G>A