Canonical Allele Identifier: CA004471
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67187
ClinVar RCV Id: RCV000057894
dbSNP Id: rs199472838

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150974886G>C , CM000669.2:g.150974886G>C GRCh38
NC_000007.13:g.150671974G>C , CM000669.1:g.150671974G>C GRCh37
NC_000007.12:g.150302907G>C NCBI36
NG_008916.1:g.8041C>G , LRG_288:g.8041C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262186.10:c.132C>G MANE Select ENSP00000262186.5:p.Cys44Trp
ENST00000262186.9:c.132C>G ENSP00000262186.5:p.Cys44Trp
ENST00000430723.4:c.-46C>G ENSP00000387657.4:n.-46C>G
ENST00000532957.5:n.355C>G
NM_000238.3:c.132C>G , LRG_288t1:c.132C>G NP_000229.1:p.Cys44Trp
NM_172056.2:c.132C>G , LRG_288t2:c.132C>G NP_742053.1:p.Cys44Trp
XM_011516186.1:c.132C>G XP_011514488.1:p.Cys44Trp
XM_011516186.3:c.132C>G XP_011514488.1:p.Cys44Trp
XM_017012196.1:c.-46C>G XP_016867685.1:n.-46C>G
NM_000238.4:c.132C>G MANE Select NP_000229.1:p.Cys44Trp