Canonical Allele Identifier: CA369865484

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 585220
• ClinVar RCV Id: RCV000709728 ; RCV002532901
• dbSNP Id: rs1563189895
• gnomAD v4: 7-150974773-A-G
• MyVariant Identifiers: chr7:g.150671861A>G (hg19) ; chr7:g.150974773A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974773A>G , CM000669.2:g.150974773A>G	GRCh38
NC_000007.13:g.150671861A>G , CM000669.1:g.150671861A>G	GRCh37
NC_000007.12:g.150302794A>G	NCBI36
NG_008916.1:g.8154T>C , LRG_288:g.8154T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.245T>C MANE Select	ENSP00000262186.5:p.Ile82Thr
ENST00000262186.9:c.245T>C	ENSP00000262186.5:p.Ile82Thr
ENST00000430723.4:c.68T>C	ENSP00000387657.4:p.Ile23Thr
ENST00000532957.5:n.468T>C
NM_000238.3:c.245T>C , LRG_288t1:c.245T>C	NP_000229.1:p.Ile82Thr
NM_172056.2:c.245T>C , LRG_288t2:c.245T>C	NP_742053.1:p.Ile82Thr
XM_011516186.1:c.245T>C	XP_011514488.1:p.Ile82Thr
XM_011516186.3:c.245T>C	XP_011514488.1:p.Ile82Thr
XM_017012196.1:c.68T>C	XP_016867685.1:p.Ile23Thr
NM_000238.4:c.245T>C MANE Select	NP_000229.1:p.Ile82Thr