LDH info

Canonical Allele Identifier: CA12735522
Gene: ZFPM2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2622633

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105497747G>A , CM000670.2:g.105497747G>A GRCh38
NC_000008.10:g.106509975G>A , CM000670.1:g.106509975G>A GRCh37
NC_000008.9:g.106579151G>A NCBI36
NG_011723.1:g.183829G>A
NG_011723.2:g.183829G>A

Transcript Alleles

HGVS Amino-acid change
NM_012082.3:c.301+53366G>A VV NP_036214.2:p.=
XM_011516946.1:c.340+53366G>A XP_011515248.1:p.=
XM_011516947.1:c.271+53366G>A XP_011515249.1:p.=
XM_011516948.1:c.142+53366G>A XP_011515250.1:p.=
XM_011516949.1:c.340+53366G>A XP_011515251.1:p.=
NM_001362836.1:c.142+53366G>A VV NP_001349765.1:p.=
NM_001362837.1:c.-96+53366G>A VV NP_001349766.1:p.=
XM_011516947.3:c.271+53366G>A XP_011515249.1:p.=
NM_012082.4:c.301+53366G>A VV MANE Preferred NP_036214.2:p.=
ENST00000407775.6:c.301+53366G>A ENSP00000384179.2:p.=
ENST00000511341.6:n.1041+53366G>A
ENST00000520027.5:c.-96+53366G>A ENSP00000428149.1:p.=
ENST00000520492.5:c.-96+53366G>A ENSP00000430757.1:p.=
ENST00000524235.5:n.514+53366G>A