LDH info

Canonical Allele Identifier: CA10654828
Gene: KCNQ2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 369751
ClinVar RCV Id: RCV000678126
dbSNP Id: rs1057516083

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63444783C>A , CM000682.2:g.63444783C>A GRCh38
NC_000020.10:g.62076136C>A , CM000682.1:g.62076136C>A GRCh37
NC_000020.9:g.61546580C>A NCBI36
NG_009004.1:g.32858G>T
NG_009004.2:g.32858G>T

Transcript Alleles

HGVS Amino-acid change
NM_004518.4:c.566G>T VV NP_004509.2:p.Gly189Val
NM_172106.1:c.566G>T VV NP_742104.1:p.Gly189Val
NM_172107.2:c.566G>T VV NP_742105.1:p.Gly189Val
NM_172108.3:c.566G>T VV NP_742106.1:p.Gly189Val
NM_172109.1:c.566G>T VV NP_742107.1:p.Gly189Val
XM_006723787.1:c.566G>T XP_006723850.1:p.Gly189Val
XM_011528807.1:c.566G>T XP_011527109.1:p.Gly189Val
XM_011528808.1:c.566G>T XP_011527110.1:p.Gly189Val
XM_011528809.1:c.566G>T XP_011527111.1:p.Gly189Val
XM_011528810.1:c.566G>T XP_011527112.1:p.Gly189Val
XM_011528811.1:c.566G>T XP_011527113.1:p.Gly189Val
XM_011528812.1:c.566G>T XP_011527114.1:p.Gly189Val
XM_011528813.1:c.566G>T XP_011527115.1:p.Gly189Val
XM_011528814.1:c.47G>T XP_011527116.1:p.Gly16Val
XM_011528815.1:c.566G>T XP_011527117.1:p.Gly189Val
XM_011528816.1:c.566G>T XP_011527118.1:p.Gly189Val
NM_004518.5:c.566G>T VV NP_004509.2:p.Gly189Val
NM_172106.2:c.566G>T VV NP_742104.1:p.Gly189Val
NM_172107.3:c.566G>T VV NP_742105.1:p.Gly189Val
NM_172108.4:c.566G>T VV NP_742106.1:p.Gly189Val
NM_172109.2:c.566G>T VV NP_742107.1:p.Gly189Val
XM_011528810.2:c.566G>T XP_011527112.1:p.Gly189Val
XM_011528811.2:c.566G>T XP_011527113.1:p.Gly189Val
XM_017027841.2:c.566G>T XP_016883330.1:p.Gly189Val
XM_017027842.2:c.566G>T XP_016883331.1:p.Gly189Val
XM_017027843.1:c.497G>T XP_016883332.1:p.Gly166Val
XM_017027844.2:c.566G>T XP_016883333.1:p.Gly189Val
ENST00000344425.7:c.566G>T ENSP00000345523.5:p.Gly189Val
ENST00000344462.8:c.566G>T ENSP00000339611.4:p.Gly189Val
ENST00000357249.6:n.224G>T ENSP00000349789.3:p.Gly75Val
ENST00000359125.6:c.566G>T ENSP00000352035.2:p.Gly189Val
ENST00000360480.7:c.566G>T ENSP00000353668.3:p.Gly189Val
ENST00000370221.3:n.692G>T
ENST00000370224.5:c.566G>T ENSP00000359244.2:p.Gly189Val
ENST00000625514.2:c.566G>T ENSP00000486040.1:p.Gly189Val
ENST00000626313.1:n.408G>T
ENST00000626839.2:c.566G>T ENSP00000486706.1:p.Gly189Val
ENST00000629241.2:c.566G>T ENSP00000487142.1:p.Gly189Val
ENST00000629676.2:c.566G>T ENSP00000486194.1:p.Gly189Val
ENST00000630274.2:n.391G>T