Canonical Allele Identifier: CA005743
Gene: KCNH2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 67304
dbSNP Id: rs199472953

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951517C>T , CM000669.2:g.150951517C>T GRCh38
NC_000007.13:g.150648605C>T , CM000669.1:g.150648605C>T GRCh37
NC_000007.12:g.150279538C>T NCBI36
NG_008916.1:g.31410G>A , LRG_288:g.31410G>A

Transcript Alleles

HGVS Amino-acid change
NM_000238.3:c.1876G>A , LRG_288t1:c.1876G>A NP_000229.1:p.Gly626Ser
NM_001204798.1:c.856G>A VV NP_001191727.1:p.Gly286Ser
NM_172056.2:c.1876G>A , LRG_288t2:c.1876G>A NP_742053.1:p.Gly626Ser
NM_172057.2:c.856G>A , LRG_288t3:c.856G>A NP_742054.1:p.Gly286Ser
XM_011516185.1:c.1576G>A XP_011514487.1:p.Gly526Ser
XM_011516186.1:c.1876G>A XP_011514488.1:p.Gly626Ser
XM_011516185.2:c.1576G>A XP_011514487.1:p.Gly526Ser
XM_011516186.3:c.1876G>A XP_011514488.1:p.Gly626Ser
XM_017012195.1:c.1726G>A XP_016867684.1:p.Gly576Ser
XM_017012196.1:c.1699G>A XP_016867685.1:p.Gly567Ser
ENST00000262186.9:c.1876G>A ENSP00000262186.5:p.Gly626Ser
ENST00000330883.8:c.856G>A ENSP00000328531.4:p.Gly286Ser
ENST00000430723.4:c.1528G>A ENSP00000387657.4:p.Gly510Ser
ENST00000461280.1:n.1163G>A
ENST00000473610.5:n.1181G>A
ENST00000532957.5:n.2099G>A