Canonical Allele Identifier: CA027465

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 927212
• ClinVar RCV Id: RCV001411395 ; RCV001841105 ; RCV002379733
• dbSNP Id: rs766849710
• ExAC: 7:150649828 G / A
• gnomAD v2: 7-150649828-G-A
• gnomAD v4: 7-150952740-G-A
• MyVariant Identifiers: chr7:g.150649828G>A (hg19) ; chr7:g.150952740G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952740G>A , CM000669.2:g.150952740G>A	GRCh38
NC_000007.13:g.150649828G>A , CM000669.1:g.150649828G>A	GRCh37
NC_000007.12:g.150280761G>A	NCBI36
NG_008916.1:g.30187C>T , LRG_288:g.30187C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.540C>T
ENST00000684116.1:n.135C>T
ENST00000684241.1:n.2075C>T
ENST00000262186.10:c.1242C>T MANE Select	ENSP00000262186.5:p.Ile414=
ENST00000330883.9:c.222C>T	ENSP00000328531.4:p.Ile74=
ENST00000262186.9:c.1242C>T	ENSP00000262186.5:p.Ile414=
ENST00000330883.8:c.222C>T	ENSP00000328531.4:p.Ile74=
ENST00000430723.4:c.894C>T	ENSP00000387657.4:p.Ile298=
ENST00000461280.1:n.529C>T
ENST00000473610.5:n.547C>T
ENST00000532957.5:n.1465C>T
NM_000238.3:c.1242C>T , LRG_288t1:c.1242C>T	NP_000229.1:p.Ile414=
NM_001204798.1:c.222C>T	NP_001191727.1:p.Ile74=
NM_172056.2:c.1242C>T , LRG_288t2:c.1242C>T	NP_742053.1:p.Ile414=
NM_172057.2:c.222C>T , LRG_288t3:c.222C>T	NP_742054.1:p.Ile74=
XM_011516185.1:c.942C>T	XP_011514487.1:p.Ile314=
XM_011516186.1:c.1242C>T	XP_011514488.1:p.Ile414=
XM_011516185.2:c.942C>T	XP_011514487.1:p.Ile314=
XM_011516186.3:c.1242C>T	XP_011514488.1:p.Ile414=
XM_017012195.1:c.1092C>T	XP_016867684.1:p.Ile364=
XM_017012196.1:c.1065C>T	XP_016867685.1:p.Ile355=
NM_000238.4:c.1242C>T MANE Select	NP_000229.1:p.Ile414=
NM_001204798.2:c.222C>T	NP_001191727.1:p.Ile74=
NM_172057.3:c.222C>T	NP_742054.1:p.Ile74=