Canonical Allele Identifier: CA458871871

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 1763383
• ClinVar RCV Id: RCV002414362
• gnomAD v4: 7-150958132-G-T
• MyVariant Identifiers: chr7:g.150655220G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958132G>T , CM000669.2:g.150958132G>T	GRCh38
NC_000007.13:g.150655220G>T , CM000669.1:g.150655220G>T	GRCh37
NC_000007.12:g.150286153G>T	NCBI36
NG_008916.1:g.24795C>A , LRG_288:g.24795C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1676C>A
ENST00000262186.10:c.843C>A MANE Select	ENSP00000262186.5:p.Arg281=
ENST00000262186.9:c.843C>A	ENSP00000262186.5:p.Arg281=
ENST00000430723.4:c.495C>A	ENSP00000387657.4:p.Arg165=
ENST00000532957.5:n.1066C>A
NM_000238.3:c.843C>A , LRG_288t1:c.843C>A	NP_000229.1:p.Arg281=
NM_172056.2:c.843C>A , LRG_288t2:c.843C>A	NP_742053.1:p.Arg281=
XM_011516185.1:c.543C>A	XP_011514487.1:p.Arg181=
XM_011516186.1:c.843C>A	XP_011514488.1:p.Arg281=
XM_011516185.2:c.543C>A	XP_011514487.1:p.Arg181=
XM_011516186.3:c.843C>A	XP_011514488.1:p.Arg281=
XM_017012195.1:c.693C>A	XP_016867684.1:p.Arg231=
XM_017012196.1:c.666C>A	XP_016867685.1:p.Arg222=
NM_000238.4:c.843C>A MANE Select	NP_000229.1:p.Arg281=