Canonical Allele Identifier: CA579075267

Gene: KCNH2

Linked Data

• dbSNP Id: rs1405010505
• gnomAD v2: 7-150655114-G-A
• gnomAD v4: 7-150958026-G-A
• MyVariant Identifiers: chr7:g.150655114G>A (hg19) ; chr7:g.150958026G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958026G>A , CM000669.2:g.150958026G>A	GRCh38
NC_000007.13:g.150655114G>A , CM000669.1:g.150655114G>A	GRCh37
NC_000007.12:g.150286047G>A	NCBI36
NG_008916.1:g.24901C>T , LRG_288:g.24901C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1749+33C>T
ENST00000262186.10:c.916+33C>T MANE Select	ENSP00000262186.5:n.916+33C>T
ENST00000262186.9:c.916+33C>T	ENSP00000262186.5:n.916+33C>T
ENST00000430723.4:c.568+33C>T	ENSP00000387657.4:n.568+33C>T
ENST00000532957.5:n.1139+33C>T
NM_000238.3:c.916+33C>T , LRG_288t1:c.916+33C>T	NP_000229.1:n.916+33C>T
NM_172056.2:c.916+33C>T , LRG_288t2:c.916+33C>T	NP_742053.1:n.916+33C>T
XM_011516185.1:c.616+33C>T	XP_011514487.1:n.616+33C>T
XM_011516186.1:c.916+33C>T	XP_011514488.1:n.916+33C>T
XM_011516185.2:c.616+33C>T	XP_011514487.1:n.616+33C>T
XM_011516186.3:c.916+33C>T	XP_011514488.1:n.916+33C>T
XM_017012195.1:c.766+33C>T	XP_016867684.1:n.766+33C>T
XM_017012196.1:c.739+33C>T	XP_016867685.1:n.739+33C>T
NM_000238.4:c.916+33C>T MANE Select	NP_000229.1:n.916+33C>T