LDH info

Canonical Allele Identifier: CA13511767
Gene: PKNOX2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10893366

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.125308507C>T , CM000673.2:g.125308507C>T GRCh38
NC_000011.9:g.125178403C>T , CM000673.1:g.125178403C>T GRCh37
NC_000011.8:g.124683613C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_022062.2:c.-129-23312C>T VV NP_071345.2:p.=
XM_005271642.1:c.-129-23312C>T XP_005271699.1:p.=
XM_006718894.1:c.-356-23312C>T XP_006718957.1:p.=
XM_011542944.1:c.-129-23312C>T XP_011541246.1:p.=
XM_011542945.1:c.-202-23312C>T XP_011541247.1:p.=
XM_011542946.1:c.-129-23312C>T XP_011541248.1:p.=
XM_011542947.1:c.-249-42777C>T XP_011541249.1:p.=
XM_005271642.2:c.-129-23312C>T XP_005271699.1:p.=
XM_006718894.2:c.-356-23312C>T XP_006718957.1:p.=
XM_011542945.2:c.-202-23312C>T XP_011541247.1:p.=
XM_011542947.2:c.-249-42777C>T XP_011541249.1:p.=
XM_017018110.1:c.-129-23312C>T XP_016873599.1:p.=
XM_017018111.1:c.-247-23312C>T XP_016873600.1:p.=
XM_024448643.1:c.-129-23312C>T XP_024304411.1:p.=
XM_024448644.1:c.-129-23312C>T XP_024304412.1:p.=
XM_024448645.1:c.-129-23312C>T XP_024304413.1:p.=
XM_024448646.1:c.-202-23312C>T XP_024304414.1:p.=
XM_024448647.1:c.-22-42777C>T XP_024304415.1:p.=
XM_024448648.1:c.-107-23312C>T XP_024304416.1:p.=
XM_024448649.1:c.-107-23312C>T XP_024304417.1:p.=
XM_024448650.1:c.-107-23312C>T XP_024304418.1:p.=
XM_024448651.1:c.-107-23312C>T XP_024304419.1:p.=
NM_022062.3:c.-129-23312C>T VV NP_071345.2:p.=
ENST00000298282.13:c.-129-23312C>T ENSP00000298282.8:p.=
ENST00000527238.5:c.-202-23312C>T ENSP00000431599.1:p.=
ENST00000530517.5:n.162-23312C>T
ENST00000531116.5:n.83-23312C>T
ENST00000531212.5:c.-129-23312C>T ENSP00000434255.1:p.=
ENST00000532623.5:c.-129-23312C>T ENSP00000434377.1:p.=
ENST00000557814.5:n.121-42777C>T
ENST00000558729.5:n.207-23312C>T
ENST00000559662.5:n.123-23312C>T
ENST00000561115.5:n.197-23312C>T