Canonical Allele Identifier: CA005433
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67267
ClinVar RCV Id: RCV000057982
dbSNP Id: rs199472929
MyVariant Identifiers: chr7:g.150648712C>A (hg19) chr7:g.150951624C>A (hg38)
PubMed: PMID:18441445 PMID:22581653
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951624C>A , CM000669.2:g.150951624C>A GRCh38
NC_000007.13:g.150648712C>A , CM000669.1:g.150648712C>A GRCh37
NC_000007.12:g.150279645C>A NCBI36
NG_008916.1:g.31303G>T , LRG_288:g.31303G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1067G>T
ENST00000684241.1:n.2602G>T
ENST00000262186.10:c.1769G>T MANE Select ENSP00000262186.5:p.Gly590Val
ENST00000330883.9:c.749G>T ENSP00000328531.4:p.Gly250Val
ENST00000262186.9:c.1769G>T ENSP00000262186.5:p.Gly590Val
ENST00000330883.8:c.749G>T ENSP00000328531.4:p.Gly250Val
ENST00000430723.4:c.1421G>T ENSP00000387657.4:p.Gly474Val
ENST00000461280.1:n.1056G>T
ENST00000473610.5:n.1074G>T
ENST00000532957.5:n.1992G>T
NM_000238.3:c.1769G>T , LRG_288t1:c.1769G>T NP_000229.1:p.Gly590Val
NM_001204798.1:c.749G>T NP_001191727.1:p.Gly250Val
NM_172056.2:c.1769G>T , LRG_288t2:c.1769G>T NP_742053.1:p.Gly590Val
NM_172057.2:c.749G>T , LRG_288t3:c.749G>T NP_742054.1:p.Gly250Val
XM_011516185.1:c.1469G>T XP_011514487.1:p.Gly490Val
XM_011516186.1:c.1769G>T XP_011514488.1:p.Gly590Val
XM_011516185.2:c.1469G>T XP_011514487.1:p.Gly490Val
XM_011516186.3:c.1769G>T XP_011514488.1:p.Gly590Val
XM_017012195.1:c.1619G>T XP_016867684.1:p.Gly540Val
XM_017012196.1:c.1592G>T XP_016867685.1:p.Gly531Val
NM_000238.4:c.1769G>T MANE Select NP_000229.1:p.Gly590Val
NM_001204798.2:c.749G>T NP_001191727.1:p.Gly250Val
NM_172057.3:c.749G>T NP_742054.1:p.Gly250Val
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