Canonical Allele Identifier: CA369865509

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 2890968
• ClinVar RCV Id: RCV003648807
• gnomAD v4: 7-150974780-C-A
• MyVariant Identifiers: chr7:g.150671868C>A (hg19) ; chr7:g.150974780C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974780C>A , CM000669.2:g.150974780C>A	GRCh38
NC_000007.13:g.150671868C>A , CM000669.1:g.150671868C>A	GRCh37
NC_000007.12:g.150302801C>A	NCBI36
NG_008916.1:g.8147G>T , LRG_288:g.8147G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.238G>T MANE Select	ENSP00000262186.5:p.Ala80Ser
ENST00000262186.9:c.238G>T	ENSP00000262186.5:p.Ala80Ser
ENST00000430723.4:c.61G>T	ENSP00000387657.4:p.Ala21Ser
ENST00000532957.5:n.461G>T
NM_000238.3:c.238G>T , LRG_288t1:c.238G>T	NP_000229.1:p.Ala80Ser
NM_172056.2:c.238G>T , LRG_288t2:c.238G>T	NP_742053.1:p.Ala80Ser
XM_011516186.1:c.238G>T	XP_011514488.1:p.Ala80Ser
XM_011516186.3:c.238G>T	XP_011514488.1:p.Ala80Ser
XM_017012196.1:c.61G>T	XP_016867685.1:p.Ala21Ser
NM_000238.4:c.238G>T MANE Select	NP_000229.1:p.Ala80Ser