Canonical Allele Identifier: CA005614
Gene: KCNH2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 67289
ClinVar RCV Id: RCV000058005
dbSNP Id: rs199472940

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951567T>C , CM000669.2:g.150951567T>C GRCh38
NC_000007.13:g.150648655T>C , CM000669.1:g.150648655T>C GRCh37
NC_000007.12:g.150279588T>C NCBI36
NG_008916.1:g.31360A>G , LRG_288:g.31360A>G

Transcript Alleles

HGVS Amino-acid change
NM_000238.3:c.1826A>G , LRG_288t1:c.1826A>G NP_000229.1:p.Asp609Gly
NM_001204798.1:c.806A>G VV NP_001191727.1:p.Asp269Gly
NM_172056.2:c.1826A>G , LRG_288t2:c.1826A>G NP_742053.1:p.Asp609Gly
NM_172057.2:c.806A>G , LRG_288t3:c.806A>G NP_742054.1:p.Asp269Gly
XM_011516185.1:c.1526A>G XP_011514487.1:p.Asp509Gly
XM_011516186.1:c.1826A>G XP_011514488.1:p.Asp609Gly
XM_011516185.2:c.1526A>G XP_011514487.1:p.Asp509Gly
XM_011516186.3:c.1826A>G XP_011514488.1:p.Asp609Gly
XM_017012195.1:c.1676A>G XP_016867684.1:p.Asp559Gly
XM_017012196.1:c.1649A>G XP_016867685.1:p.Asp550Gly
ENST00000262186.9:c.1826A>G ENSP00000262186.5:p.Asp609Gly
ENST00000330883.8:c.806A>G ENSP00000328531.4:p.Asp269Gly
ENST00000430723.4:c.1478A>G ENSP00000387657.4:p.Asp493Gly
ENST00000461280.1:n.1113A>G
ENST00000473610.5:n.1131A>G
ENST00000532957.5:n.2049A>G