Canonical Allele Identifier: CA369862862

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958298-C-A
• MyVariant Identifiers: chr7:g.150655386C>A (hg19) ; chr7:g.150958298C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958298C>A , CM000669.2:g.150958298C>A	GRCh38
NC_000007.13:g.150655386C>A , CM000669.1:g.150655386C>A	GRCh37
NC_000007.12:g.150286319C>A	NCBI36
NG_008916.1:g.24629G>T , LRG_288:g.24629G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1510G>T
ENST00000262186.10:c.677G>T MANE Select	ENSP00000262186.5:p.Gly226Val
ENST00000262186.9:c.677G>T	ENSP00000262186.5:p.Gly226Val
ENST00000430723.4:c.329G>T	ENSP00000387657.4:p.Gly110Val
ENST00000532957.5:n.900G>T
NM_000238.3:c.677G>T , LRG_288t1:c.677G>T	NP_000229.1:p.Gly226Val
NM_172056.2:c.677G>T , LRG_288t2:c.677G>T	NP_742053.1:p.Gly226Val
XM_011516185.1:c.377G>T	XP_011514487.1:p.Gly126Val
XM_011516186.1:c.677G>T	XP_011514488.1:p.Gly226Val
XM_011516185.2:c.377G>T	XP_011514487.1:p.Gly126Val
XM_011516186.3:c.677G>T	XP_011514488.1:p.Gly226Val
XM_017012195.1:c.527G>T	XP_016867684.1:p.Gly176Val
XM_017012196.1:c.500G>T	XP_016867685.1:p.Gly167Val
NM_000238.4:c.677G>T MANE Select	NP_000229.1:p.Gly226Val