Canonical Allele Identifier: CA369853457

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150644905A>C (hg19) ; chr7:g.150947817A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947817A>C , CM000669.2:g.150947817A>C	GRCh38
NC_000007.13:g.150644905A>C , CM000669.1:g.150644905A>C	GRCh37
NC_000007.12:g.150275838A>C	NCBI36
NG_008916.1:g.35110T>G , LRG_288:g.35110T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3587T>G
ENST00000262186.10:c.2754T>G MANE Select	ENSP00000262186.5:p.Ser918Arg
ENST00000330883.9:c.1734T>G	ENSP00000328531.4:p.Ser578Arg
ENST00000262186.9:c.2754T>G	ENSP00000262186.5:p.Ser918Arg
ENST00000330883.8:c.1734T>G	ENSP00000328531.4:p.Ser578Arg
NM_000238.3:c.2754T>G , LRG_288t1:c.2754T>G	NP_000229.1:p.Ser918Arg
NM_172057.2:c.1734T>G , LRG_288t3:c.1734T>G	NP_742054.1:p.Ser578Arg
XM_011516185.1:c.2454T>G	XP_011514487.1:p.Ser818Arg
XM_011516186.1:c.2693-126T>G	XP_011514488.1:n.2693-126T>G
XM_011516185.2:c.2454T>G	XP_011514487.1:p.Ser818Arg
XM_011516186.3:c.2693-126T>G	XP_011514488.1:n.2693-126T>G
XM_017012195.1:c.2604T>G	XP_016867684.1:p.Ser868Arg
XM_017012196.1:c.2577T>G	XP_016867685.1:p.Ser859Arg
NM_000238.4:c.2754T>G MANE Select	NP_000229.1:p.Ser918Arg
NM_172057.3:c.1734T>G	NP_742054.1:p.Ser578Arg