Canonical Allele Identifier: CA1752417714
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150958070T= , CM000669.2:g.150958070T= GRCh38
NC_000007.13:g.150655158T= , CM000669.1:g.150655158T= GRCh37
NC_000007.12:g.150286091T= NCBI36
NG_008916.1:g.24857A= , LRG_288:g.24857A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1738A=
ENST00000262186.10:c.905A= MANE Select ENSP00000262186.5:p.His302=
ENST00000262186.9:c.905A= ENSP00000262186.5:p.His302=
ENST00000430723.4:c.557A= ENSP00000387657.4:p.His186=
ENST00000532957.5:n.1128A=
NM_000238.3:c.905A= , LRG_288t1:c.905A= NP_000229.1:p.His302=
NM_172056.2:c.905A= , LRG_288t2:c.905A= NP_742053.1:p.His302=
XM_011516185.1:c.605A= XP_011514487.1:p.His202=
XM_011516186.1:c.905A= XP_011514488.1:p.His302=
XM_011516185.2:c.605A= XP_011514487.1:p.His202=
XM_011516186.3:c.905A= XP_011514488.1:p.His302=
XM_017012195.1:c.755A= XP_016867684.1:p.His252=
XM_017012196.1:c.728A= XP_016867685.1:p.His243=
NM_000238.4:c.905A= MANE Select NP_000229.1:p.His302=