Canonical Allele Identifier: CA005600

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 67287
• ClinVar RCV Id: RCV000058003
• dbSNP Id: rs199472941
• MyVariant Identifiers: chr7:g.150648656C>G (hg19) ; chr7:g.150951568C>G (hg38)
• PubMed: PMID:16414944 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951568C>G , CM000669.2:g.150951568C>G	GRCh38
NC_000007.13:g.150648656C>G , CM000669.1:g.150648656C>G	GRCh37
NC_000007.12:g.150279589C>G	NCBI36
NG_008916.1:g.31359G>C , LRG_288:g.31359G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1123G>C
ENST00000684241.1:n.2658G>C
ENST00000262186.10:c.1825G>C MANE Select	ENSP00000262186.5:p.Asp609His
ENST00000330883.9:c.805G>C	ENSP00000328531.4:p.Asp269His
ENST00000262186.9:c.1825G>C	ENSP00000262186.5:p.Asp609His
ENST00000330883.8:c.805G>C	ENSP00000328531.4:p.Asp269His
ENST00000430723.4:c.1477G>C	ENSP00000387657.4:p.Asp493His
ENST00000461280.1:n.1112G>C
ENST00000473610.5:n.1130G>C
ENST00000532957.5:n.2048G>C
NM_000238.3:c.1825G>C , LRG_288t1:c.1825G>C	NP_000229.1:p.Asp609His
NM_001204798.1:c.805G>C	NP_001191727.1:p.Asp269His
NM_172056.2:c.1825G>C , LRG_288t2:c.1825G>C	NP_742053.1:p.Asp609His
NM_172057.2:c.805G>C , LRG_288t3:c.805G>C	NP_742054.1:p.Asp269His
XM_011516185.1:c.1525G>C	XP_011514487.1:p.Asp509His
XM_011516186.1:c.1825G>C	XP_011514488.1:p.Asp609His
XM_011516185.2:c.1525G>C	XP_011514487.1:p.Asp509His
XM_011516186.3:c.1825G>C	XP_011514488.1:p.Asp609His
XM_017012195.1:c.1675G>C	XP_016867684.1:p.Asp559His
XM_017012196.1:c.1648G>C	XP_016867685.1:p.Asp550His
NM_000238.4:c.1825G>C MANE Select	NP_000229.1:p.Asp609His
NM_001204798.2:c.805G>C	NP_001191727.1:p.Asp269His
NM_172057.3:c.805G>C	NP_742054.1:p.Asp269His