LDH info

Canonical Allele Identifier: CA15696918
Gene: PDE3B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1007392

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14753045A>G , CM000673.2:g.14753045A>G GRCh38
NC_000011.9:g.14774591A>G , CM000673.1:g.14774591A>G GRCh37
NC_000011.8:g.14731167A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_000922.3:c.979-18892A>G VV NP_000913.2:p.=
XM_006718249.2:c.979-18892A>G XP_006718312.1:p.=
XM_011520183.1:c.979-18892A>G XP_011518485.1:p.=
NM_001363569.1:c.979-18892A>G VV NP_001350498.1:p.=
NM_001363570.1:c.979-18892A>G VV NP_001350499.1:p.=
XM_006718249.3:c.979-18892A>G XP_006718312.1:p.=
XM_017017911.2:c.979-18892A>G XP_016873400.1:p.=
XM_017017912.1:c.979-18892A>G XP_016873401.1:p.=
XR_001747903.2:n.1364-18892A>G
NM_000922.4:c.979-18892A>G VV MANE Preferred NP_000913.2:p.=
ENST00000282096.8:c.979-18892A>G ENSP00000282096.4:p.=
ENST00000455098.2:c.979-18892A>G ENSP00000388644.2:p.=
ENST00000534317.1:n.795-18892A>G