Canonical Allele Identifier: CA369865832

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 1303967
• ClinVar RCV Id: RCV001758260 ; RCV002032795
• dbSNP Id: rs2117063507
• MyVariant Identifiers: chr7:g.150671969T>C (hg19) ; chr7:g.150974881T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974881T>C , CM000669.2:g.150974881T>C	GRCh38
NC_000007.13:g.150671969T>C , CM000669.1:g.150671969T>C	GRCh37
NC_000007.12:g.150302902T>C	NCBI36
NG_008916.1:g.8046A>G , LRG_288:g.8046A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.137A>G MANE Select	ENSP00000262186.5:p.Asp46Gly
ENST00000262186.9:c.137A>G	ENSP00000262186.5:p.Asp46Gly
ENST00000430723.4:c.-41A>G	ENSP00000387657.4:n.-41A>G
ENST00000532957.5:n.360A>G
NM_000238.3:c.137A>G , LRG_288t1:c.137A>G	NP_000229.1:p.Asp46Gly
NM_172056.2:c.137A>G , LRG_288t2:c.137A>G	NP_742053.1:p.Asp46Gly
XM_011516186.1:c.137A>G	XP_011514488.1:p.Asp46Gly
XM_011516186.3:c.137A>G	XP_011514488.1:p.Asp46Gly
XM_017012196.1:c.-41A>G	XP_016867685.1:n.-41A>G
NM_000238.4:c.137A>G MANE Select	NP_000229.1:p.Asp46Gly