Canonical Allele Identifier: CA028209

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 456889
• ClinVar RCV Id: RCV000525629 ; RCV000619850
• dbSNP Id: rs147126965
• ExAC: 7:150649570 G / A
• gnomAD v2: 7-150649570-G-A
• gnomAD v3: 7-150952482-G-A
• gnomAD v4: 7-150952482-G-A
• MyVariant Identifiers: chr7:g.150649570G>A (hg19) ; chr7:g.150952482G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952482G>A , CM000669.2:g.150952482G>A	GRCh38
NC_000007.13:g.150649570G>A , CM000669.1:g.150649570G>A	GRCh37
NC_000007.12:g.150280503G>A	NCBI36
NG_008916.1:g.30445C>T , LRG_288:g.30445C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.798C>T
ENST00000684116.1:n.393C>T
ENST00000684241.1:n.2333C>T
ENST00000262186.10:c.1500C>T MANE Select	ENSP00000262186.5:p.Ile500=
ENST00000330883.9:c.480C>T	ENSP00000328531.4:p.Ile160=
ENST00000262186.9:c.1500C>T	ENSP00000262186.5:p.Ile500=
ENST00000330883.8:c.480C>T	ENSP00000328531.4:p.Ile160=
ENST00000430723.4:c.1152C>T	ENSP00000387657.4:p.Ile384=
ENST00000461280.1:n.787C>T
ENST00000473610.5:n.805C>T
ENST00000532957.5:n.1723C>T
NM_000238.3:c.1500C>T , LRG_288t1:c.1500C>T	NP_000229.1:p.Ile500=
NM_001204798.1:c.480C>T	NP_001191727.1:p.Ile160=
NM_172056.2:c.1500C>T , LRG_288t2:c.1500C>T	NP_742053.1:p.Ile500=
NM_172057.2:c.480C>T , LRG_288t3:c.480C>T	NP_742054.1:p.Ile160=
XM_011516185.1:c.1200C>T	XP_011514487.1:p.Ile400=
XM_011516186.1:c.1500C>T	XP_011514488.1:p.Ile500=
XM_011516185.2:c.1200C>T	XP_011514487.1:p.Ile400=
XM_011516186.3:c.1500C>T	XP_011514488.1:p.Ile500=
XM_017012195.1:c.1350C>T	XP_016867684.1:p.Ile450=
XM_017012196.1:c.1323C>T	XP_016867685.1:p.Ile441=
NM_000238.4:c.1500C>T MANE Select	NP_000229.1:p.Ile500=
NM_001204798.2:c.480C>T	NP_001191727.1:p.Ile160=
NM_172057.3:c.480C>T	NP_742054.1:p.Ile160=