LDH info

Canonical Allele Identifier: CA14026418
Gene: PPP2R3C HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2038255

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35089920C>T , CM000676.2:g.35089920C>T GRCh38
NC_000014.8:g.35559126C>T , CM000676.1:g.35559126C>T GRCh37
NC_000014.7:g.34628877C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001305155.1:c.783+1150G>A VV NP_001292084.1:p.=
NM_001305156.1:c.783+1150G>A VV NP_001292085.1:p.=
NM_017917.2:c.1113+1150G>A VV NP_060387.2:p.=
NM_017917.3:c.1113+1150G>A VV NP_060387.2:p.=
NR_110415.1:n.479+8361C>T
NR_130972.1:n.1312+1150G>A
XM_005267782.2:c.1113+1150G>A XP_005267839.1:p.=
XM_011536885.1:c.957+1150G>A XP_011535187.1:p.=
XM_005267782.4:c.1113+1150G>A XP_005267839.1:p.=
XM_017021388.2:c.976-1910G>A XP_016876877.1:p.=
XM_024449638.1:c.1020+1150G>A XP_024305406.1:p.=
XM_024449639.1:c.957+1150G>A XP_024305407.1:p.=
XR_002957558.1:n.1439+1150G>A
ENST00000261475.9:c.1113+1150G>A ENSP00000261475.5:p.=
ENST00000553273.5:c.*779+1150G>A ENSP00000451075.1:p.=
ENST00000554222.5:c.*916+1150G>A ENSP00000451416.1:p.=
ENST00000555219.1:n.139-1910G>A ENSP00000452173.1:p.=
ENST00000555260.1:n.479+8361C>T
ENST00000557074.1:n.110+1150G>A
ENST00000557217.5:c.*916+1150G>A ENSP00000452436.1:p.=