Canonical Allele Identifier: CA1108705549

Gene: KCNH2

Linked Data

• dbSNP Id: rs1801065570
• gnomAD v3: 7-150949850-G-A
• gnomAD v4: 7-150949850-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150949850G>A , CM000669.2:g.150949850G>A	GRCh38
NC_000007.13:g.150646938G>A , CM000669.1:g.150646938G>A	GRCh37
NC_000007.12:g.150277871G>A	NCBI36
NG_008916.1:g.33077C>T , LRG_288:g.33077C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.2014C>T
ENST00000684241.1:n.3231+318C>T
ENST00000262186.10:c.2398+318C>T MANE Select	ENSP00000262186.5:n.2398+318C>T
ENST00000330883.9:c.1378+318C>T	ENSP00000328531.4:n.1378+318C>T
ENST00000262186.9:c.2398+318C>T	ENSP00000262186.5:n.2398+318C>T
ENST00000330883.8:c.1378+318C>T	ENSP00000328531.4:n.1378+318C>T
ENST00000461280.1:n.2003C>T
ENST00000473610.5:n.2348C>T
ENST00000532957.5:n.2939C>T
NM_000238.3:c.2398+318C>T , LRG_288t1:c.2398+318C>T	NP_000229.1:n.2398+318C>T
NM_001204798.1:c.*49C>T	NP_001191727.1:n.*49C>T
NM_172056.2:c.*49C>T , LRG_288t2:c.*49C>T	NP_742053.1:n.*49C>T
NM_172057.2:c.1378+318C>T , LRG_288t3:c.1378+318C>T	NP_742054.1:n.1378+318C>T
XM_011516185.1:c.2098+318C>T	XP_011514487.1:n.2098+318C>T
XM_011516186.1:c.2398+318C>T	XP_011514488.1:n.2398+318C>T
XM_011516185.2:c.2098+318C>T	XP_011514487.1:n.2098+318C>T
XM_011516186.3:c.2398+318C>T	XP_011514488.1:n.2398+318C>T
XM_017012195.1:c.2248+318C>T	XP_016867684.1:n.2248+318C>T
XM_017012196.1:c.2221+318C>T	XP_016867685.1:n.2221+318C>T
NM_000238.4:c.2398+318C>T MANE Select	NP_000229.1:n.2398+318C>T
NM_001204798.2:c.*49C>T	NP_001191727.1:n.*49C>T
NM_172057.3:c.1378+318C>T	NP_742054.1:n.1378+318C>T