Canonical Allele Identifier: CA369865505
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1965441
ClinVar RCV Id: RCV002745270

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150974779G>C , CM000669.2:g.150974779G>C GRCh38
NC_000007.13:g.150671867G>C , CM000669.1:g.150671867G>C GRCh37
NC_000007.12:g.150302800G>C NCBI36
NG_008916.1:g.8148C>G , LRG_288:g.8148C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262186.10:c.239C>G MANE Select ENSP00000262186.5:p.Ala80Gly
ENST00000262186.9:c.239C>G ENSP00000262186.5:p.Ala80Gly
ENST00000430723.4:c.62C>G ENSP00000387657.4:p.Ala21Gly
ENST00000532957.5:n.462C>G
NM_000238.3:c.239C>G , LRG_288t1:c.239C>G NP_000229.1:p.Ala80Gly
NM_172056.2:c.239C>G , LRG_288t2:c.239C>G NP_742053.1:p.Ala80Gly
XM_011516186.1:c.239C>G XP_011514488.1:p.Ala80Gly
XM_011516186.3:c.239C>G XP_011514488.1:p.Ala80Gly
XM_017012196.1:c.62C>G XP_016867685.1:p.Ala21Gly
NM_000238.4:c.239C>G MANE Select NP_000229.1:p.Ala80Gly