LDH info

Canonical Allele Identifier: CA15759346
Gene: CLEC12B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1054611

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10017562G>T , CM000674.2:g.10017562G>T GRCh38
NC_000012.11:g.10170161G>T , CM000674.1:g.10170161G>T GRCh37
NC_000012.10:g.10061428G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001129998.1:c.681-769G>T VV NP_001123470.1:p.=
NM_205852.2:c.*1816G>T VV NP_995324.2:p.=
NR_120484.1:n.249-1789C>A
XM_006719070.2:c.681-856G>T XP_006719133.1:p.=
XM_006719071.2:c.*3-769G>T XP_006719134.1:p.=
XM_006719072.1:c.*589G>T XP_006719135.1:p.=
XM_011520658.1:c.654-769G>T XP_011518960.1:p.=
XM_011520659.1:c.*565G>T XP_011518961.1:p.=
XM_011520660.1:c.*560G>T XP_011518962.1:p.=
XM_011520661.1:c.*10-769G>T XP_011518963.1:p.=
XM_011520662.1:c.*596G>T XP_011518964.1:p.=
XM_011520663.1:c.526-769G>T XP_011518965.1:p.=
XM_011520664.1:c.526-856G>T XP_011518966.1:p.=
XR_242889.3:n.956-769G>T
XR_931290.1:n.1542G>T
NM_001129998.2:c.681-769G>T VV NP_001123470.1:p.=
NM_001319241.1:c.372-769G>T VV NP_001306170.1:p.=
NM_001319242.1:c.*1816G>T VV NP_001306171.1:p.=
NM_205852.3:c.*1816G>T VV NP_995324.2:p.=
NR_135049.1:n.961-769G>T
XM_011520658.2:c.654-769G>T XP_011518960.1:p.=
XM_011520663.2:c.526-769G>T XP_011518965.1:p.=
XM_017019295.1:c.372-769G>T XP_016874784.1:p.=
XM_024448976.1:c.681-856G>T XP_024304744.1:p.=
XM_024448977.1:c.*1823G>T XP_024304745.1:p.=
XR_002957401.1:n.106-1414C>A
ENST00000338896.9:c.681-769G>T ENSP00000344563.5:p.=
ENST00000396502.5:c.*1816G>T ENSP00000379759.1:p.=
ENST00000539155.1:c.*2309G>T ENSP00000444909.1:p.=
ENST00000544853.5:c.*129-769G>T ENSP00000439561.1:p.=