Canonical Allele Identifier: CA006942
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67412
ClinVar RCV Id: RCV000058136
dbSNP Id: rs199473539

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948875A>G , CM000669.2:g.150948875A>G GRCh38
NC_000007.13:g.150645963A>G , CM000669.1:g.150645963A>G GRCh37
NC_000007.12:g.150276896A>G NCBI36
NG_008916.1:g.34052T>C , LRG_288:g.34052T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.3406T>C
ENST00000262186.10:c.2573T>C MANE Select ENSP00000262186.5:p.Ile858Thr
ENST00000330883.9:c.1553T>C ENSP00000328531.4:p.Ile518Thr
ENST00000262186.9:c.2573T>C ENSP00000262186.5:p.Ile858Thr
ENST00000330883.8:c.1553T>C ENSP00000328531.4:p.Ile518Thr
NM_000238.3:c.2573T>C , LRG_288t1:c.2573T>C NP_000229.1:p.Ile858Thr
NM_172057.2:c.1553T>C , LRG_288t3:c.1553T>C NP_742054.1:p.Ile518Thr
XM_011516185.1:c.2273T>C XP_011514487.1:p.Ile758Thr
XM_011516186.1:c.2573T>C XP_011514488.1:p.Ile858Thr
XM_011516185.2:c.2273T>C XP_011514487.1:p.Ile758Thr
XM_011516186.3:c.2573T>C XP_011514488.1:p.Ile858Thr
XM_017012195.1:c.2423T>C XP_016867684.1:p.Ile808Thr
XM_017012196.1:c.2396T>C XP_016867685.1:p.Ile799Thr
NM_000238.4:c.2573T>C MANE Select NP_000229.1:p.Ile858Thr
NM_172057.3:c.1553T>C NP_742054.1:p.Ile518Thr