Canonical Allele Identifier: CA008669

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 200297
• ClinVar RCV Id: RCV000181764 ; RCV002503707
• dbSNP Id: rs794728358
• gnomAD v4: 7-150958305-C-T
• MyVariant Identifiers: chr7:g.150655393C>T (hg19) ; chr7:g.150958305C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958305C>T , CM000669.2:g.150958305C>T	GRCh38
NC_000007.13:g.150655393C>T , CM000669.1:g.150655393C>T	GRCh37
NC_000007.12:g.150286326C>T	NCBI36
NG_008916.1:g.24622G>A , LRG_288:g.24622G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1503G>A
ENST00000262186.10:c.670G>A MANE Select	ENSP00000262186.5:p.Gly224Arg
ENST00000262186.9:c.670G>A	ENSP00000262186.5:p.Gly224Arg
ENST00000430723.4:c.322G>A	ENSP00000387657.4:p.Gly108Arg
ENST00000532957.5:n.893G>A
NM_000238.3:c.670G>A , LRG_288t1:c.670G>A	NP_000229.1:p.Gly224Arg
NM_172056.2:c.670G>A , LRG_288t2:c.670G>A	NP_742053.1:p.Gly224Arg
XM_011516185.1:c.370G>A	XP_011514487.1:p.Gly124Arg
XM_011516186.1:c.670G>A	XP_011514488.1:p.Gly224Arg
XM_011516185.2:c.370G>A	XP_011514487.1:p.Gly124Arg
XM_011516186.3:c.670G>A	XP_011514488.1:p.Gly224Arg
XM_017012195.1:c.520G>A	XP_016867684.1:p.Gly174Arg
XM_017012196.1:c.493G>A	XP_016867685.1:p.Gly165Arg
NM_000238.4:c.670G>A MANE Select	NP_000229.1:p.Gly224Arg