Canonical Allele Identifier: CA369857574

Gene: KCNH2

Linked Data

• dbSNP Id: rs778135438
• gnomAD v3: 7-150951013-G-C
• gnomAD v4: 7-150951013-G-C
• MyVariant Identifiers: chr7:g.150648101G>C (hg19) ; chr7:g.150951013G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951013G>C , CM000669.2:g.150951013G>C	GRCh38
NC_000007.13:g.150648101G>C , CM000669.1:g.150648101G>C	GRCh37
NC_000007.12:g.150279034G>C	NCBI36
NG_008916.1:g.31914C>G , LRG_288:g.31914C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1351C>G
ENST00000683359.1:n.177C>G
ENST00000684241.1:n.2886C>G
ENST00000262186.10:c.2053C>G MANE Select	ENSP00000262186.5:p.Arg685Gly
ENST00000330883.9:c.1033C>G	ENSP00000328531.4:p.Arg345Gly
ENST00000262186.9:c.2053C>G	ENSP00000262186.5:p.Arg685Gly
ENST00000330883.8:c.1033C>G	ENSP00000328531.4:p.Arg345Gly
ENST00000430723.4:c.1705C>G	ENSP00000387657.4:p.Arg569Gly
ENST00000461280.1:n.1340C>G
ENST00000473610.5:n.1685C>G
ENST00000532957.5:n.2276C>G
NM_000238.3:c.2053C>G , LRG_288t1:c.2053C>G	NP_000229.1:p.Arg685Gly
NM_001204798.1:c.1033C>G	NP_001191727.1:p.Arg345Gly
NM_172056.2:c.2053C>G , LRG_288t2:c.2053C>G	NP_742053.1:p.Arg685Gly
NM_172057.2:c.1033C>G , LRG_288t3:c.1033C>G	NP_742054.1:p.Arg345Gly
XM_011516185.1:c.1753C>G	XP_011514487.1:p.Arg585Gly
XM_011516186.1:c.2053C>G	XP_011514488.1:p.Arg685Gly
XM_011516185.2:c.1753C>G	XP_011514487.1:p.Arg585Gly
XM_011516186.3:c.2053C>G	XP_011514488.1:p.Arg685Gly
XM_017012195.1:c.1903C>G	XP_016867684.1:p.Arg635Gly
XM_017012196.1:c.1876C>G	XP_016867685.1:p.Arg626Gly
NM_000238.4:c.2053C>G MANE Select	NP_000229.1:p.Arg685Gly
NM_001204798.2:c.1033C>G	NP_001191727.1:p.Arg345Gly
NM_172057.3:c.1033C>G	NP_742054.1:p.Arg345Gly