Canonical Allele Identifier: CA1752417012
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150957494G= , CM000669.2:g.150957494G= GRCh38
NC_000007.13:g.150654582G= , CM000669.1:g.150654582G= GRCh37
NC_000007.12:g.150285515G= NCBI36
NG_008916.1:g.25433C= , LRG_288:g.25433C=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1758C=
ENST00000262186.10:c.925C= MANE Select ENSP00000262186.5:p.His309=
ENST00000262186.9:c.925C= ENSP00000262186.5:p.His309=
ENST00000430723.4:c.577C= ENSP00000387657.4:p.His193=
ENST00000532957.5:n.1148C=
NM_000238.3:c.925C= , LRG_288t1:c.925C= NP_000229.1:p.His309=
NM_172056.2:c.925C= , LRG_288t2:c.925C= NP_742053.1:p.His309=
XM_011516185.1:c.625C= XP_011514487.1:p.His209=
XM_011516186.1:c.925C= XP_011514488.1:p.His309=
XM_011516185.2:c.625C= XP_011514487.1:p.His209=
XM_011516186.3:c.925C= XP_011514488.1:p.His309=
XM_017012195.1:c.775C= XP_016867684.1:p.His259=
XM_017012196.1:c.748C= XP_016867685.1:p.His250=
NM_000238.4:c.925C= MANE Select NP_000229.1:p.His309=