LDH info

Canonical Allele Identifier: CA15996573
Gene: COMT HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4646312

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19960814T>C , CM000684.2:g.19960814T>C GRCh38
NC_000022.10:g.19948337T>C , CM000684.1:g.19948337T>C GRCh37
NC_000022.9:g.18328337T>C NCBI36
NG_011526.1:g.24075T>C

Transcript Alleles

HGVS Amino-acid change
NM_000754.3:c.-91-385T>C VV NP_000745.1:p.=
NM_001135161.1:c.-91-385T>C VV NP_001128633.1:p.=
NM_001135162.1:c.-91-385T>C VV NP_001128634.1:p.=
XM_011529885.1:c.24-385T>C XP_011528187.1:p.=
XM_011529886.1:c.24-385T>C XP_011528188.1:p.=
XM_011529887.1:c.-91-385T>C XP_011528189.1:p.=
XM_011529888.1:c.-91-385T>C XP_011528190.1:p.=
XM_011529889.1:c.-91-385T>C XP_011528191.1:p.=
XM_011529890.1:c.-385-385T>C XP_011528192.1:p.=
XM_011529891.1:c.-385-385T>C XP_011528193.1:p.=
NM_001362828.1:c.-385-385T>C VV NP_001349757.1:p.=
XM_011529886.2:c.321-385T>C XP_011528188.2:p.=
XM_017028595.1:c.-385-385T>C XP_016884084.1:p.=
NM_000754.4:c.-91-385T>C VV MANE Preferred NP_000745.1:p.=
NM_001135161.2:c.-91-385T>C VV NP_001128633.1:p.=
NM_001135162.2:c.-91-385T>C VV NP_001128634.1:p.=
NM_001362828.2:c.-385-385T>C VV NP_001349757.1:p.=
ENST00000207636.9:c.-91-385T>C ENSP00000207636.5:p.=
ENST00000361682.10:c.-91-385T>C ENSP00000354511.6:p.=
ENST00000403184.5:c.-91-385T>C ENSP00000383966.1:p.=
ENST00000403710.5:c.-385-385T>C ENSP00000385917.1:p.=
ENST00000406520.7:c.-91-385T>C ENSP00000385150.3:p.=
ENST00000407537.5:c.-269-385T>C ENSP00000384654.2:p.=
ENST00000412786.5:c.-91-385T>C ENSP00000403958.1:p.=
ENST00000467943.5:n.106-385T>C