Canonical Allele Identifier: CA005395
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67264
ClinVar RCV Id: RCV000057977
dbSNP Id: rs199473429
MyVariant Identifiers: chr7:g.150648730C>A (hg19) chr7:g.150951642C>A (hg38)
PubMed: PMID:18752142 PMID:22581653
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951642C>A , CM000669.2:g.150951642C>A GRCh38
NC_000007.13:g.150648730C>A , CM000669.1:g.150648730C>A GRCh37
NC_000007.12:g.150279663C>A NCBI36
NG_008916.1:g.31285G>T , LRG_288:g.31285G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1049G>T
ENST00000684241.1:n.2584G>T
ENST00000262186.10:c.1751G>T MANE Select ENSP00000262186.5:p.Gly584Val
ENST00000330883.9:c.731G>T ENSP00000328531.4:p.Gly244Val
ENST00000262186.9:c.1751G>T ENSP00000262186.5:p.Gly584Val
ENST00000330883.8:c.731G>T ENSP00000328531.4:p.Gly244Val
ENST00000430723.4:c.1403G>T ENSP00000387657.4:p.Gly468Val
ENST00000461280.1:n.1038G>T
ENST00000473610.5:n.1056G>T
ENST00000532957.5:n.1974G>T
NM_000238.3:c.1751G>T , LRG_288t1:c.1751G>T NP_000229.1:p.Gly584Val
NM_001204798.1:c.731G>T NP_001191727.1:p.Gly244Val
NM_172056.2:c.1751G>T , LRG_288t2:c.1751G>T NP_742053.1:p.Gly584Val
NM_172057.2:c.731G>T , LRG_288t3:c.731G>T NP_742054.1:p.Gly244Val
XM_011516185.1:c.1451G>T XP_011514487.1:p.Gly484Val
XM_011516186.1:c.1751G>T XP_011514488.1:p.Gly584Val
XM_011516185.2:c.1451G>T XP_011514487.1:p.Gly484Val
XM_011516186.3:c.1751G>T XP_011514488.1:p.Gly584Val
XM_017012195.1:c.1601G>T XP_016867684.1:p.Gly534Val
XM_017012196.1:c.1574G>T XP_016867685.1:p.Gly525Val
NM_000238.4:c.1751G>T MANE Select NP_000229.1:p.Gly584Val
NM_001204798.2:c.731G>T NP_001191727.1:p.Gly244Val
NM_172057.3:c.731G>T NP_742054.1:p.Gly244Val
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