Canonical Allele Identifier: CA458871805

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 923150
• ClinVar RCV Id: RCV001843175 ; RCV003532884
• dbSNP Id: rs974990528
• gnomAD v2: 7-150671860-G-A
• gnomAD v4: 7-150974772-G-A
• MyVariant Identifiers: chr7:g.150671860G>A (hg19) ; chr7:g.150974772G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974772G>A , CM000669.2:g.150974772G>A	GRCh38
NC_000007.13:g.150671860G>A , CM000669.1:g.150671860G>A	GRCh37
NC_000007.12:g.150302793G>A	NCBI36
NG_008916.1:g.8155C>T , LRG_288:g.8155C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.246C>T MANE Select	ENSP00000262186.5:p.Ile82=
ENST00000262186.9:c.246C>T	ENSP00000262186.5:p.Ile82=
ENST00000430723.4:c.69C>T	ENSP00000387657.4:p.Ile23=
ENST00000532957.5:n.469C>T
NM_000238.3:c.246C>T , LRG_288t1:c.246C>T	NP_000229.1:p.Ile82=
NM_172056.2:c.246C>T , LRG_288t2:c.246C>T	NP_742053.1:p.Ile82=
XM_011516186.1:c.246C>T	XP_011514488.1:p.Ile82=
XM_011516186.3:c.246C>T	XP_011514488.1:p.Ile82=
XM_017012196.1:c.69C>T	XP_016867685.1:p.Ile23=
NM_000238.4:c.246C>T MANE Select	NP_000229.1:p.Ile82=