LDH info

Canonical Allele Identifier: CA12832981
Gene: PPP3CC HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10108011

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22463293G>A , CM000670.2:g.22463293G>A GRCh38
NC_000008.10:g.22320806G>A , CM000670.1:g.22320806G>A GRCh37
NC_000008.9:g.22376751G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001243974.1:c.50-11661G>A VV NP_001230903.1:p.=
NM_001243975.1:c.50-11661G>A VV NP_001230904.1:p.=
NM_005605.4:c.50-11661G>A VV NP_005596.2:p.=
XM_005273564.1:c.50-11661G>A XP_005273621.1:p.=
XR_949434.1:n.490-11661G>A
XR_949436.1:n.490-11661G>A
XM_017013611.2:c.50-11661G>A XP_016869100.1:p.=
XR_001745553.2:n.407-11661G>A
XR_001745554.2:n.407-11661G>A
XR_001745555.2:n.407-11661G>A
XR_001745556.2:n.407-11661G>A
XR_001745557.2:n.407-11661G>A
XR_001745558.2:n.407-11661G>A
XR_001745559.2:n.407-11661G>A
NM_001243974.2:c.50-11661G>A VV NP_001230903.1:p.=
NM_001243975.2:c.50-11661G>A VV NP_001230904.1:p.=
NM_005605.5:c.50-11661G>A VV MANE Preferred NP_005596.2:p.=
ENST00000240139.9:c.50-11661G>A ENSP00000240139.5:p.=
ENST00000289963.12:c.50-11661G>A ENSP00000289963.8:p.=
ENST00000397775.7:c.50-11661G>A ENSP00000380878.3:p.=
ENST00000518852.5:c.50-11661G>A ENSP00000429379.1:p.=
ENST00000522000.1:n.95-11661G>A ENSP00000428358.1:p.=