Canonical Allele Identifier: CA169081470

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 516110
• ClinVar RCV Id: RCV001704760 ; RCV003162751
• dbSNP Id: rs894519401
• gnomAD v2: 7-150655508-C-T
• gnomAD v3: 7-150958420-C-T
• gnomAD v4: 7-150958420-C-T
• MyVariant Identifiers: chr7:g.150655508C>T (hg19) ; chr7:g.150958420C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958420C>T , CM000669.2:g.150958420C>T	GRCh38
NC_000007.13:g.150655508C>T , CM000669.1:g.150655508C>T	GRCh37
NC_000007.12:g.150286441C>T	NCBI36
NG_008916.1:g.24507G>A , LRG_288:g.24507G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1388G>A
ENST00000262186.10:c.555G>A MANE Select	ENSP00000262186.5:p.Ala185=
ENST00000262186.9:c.555G>A	ENSP00000262186.5:p.Ala185=
ENST00000430723.4:c.235-28G>A	ENSP00000387657.4:n.235-28G>A
ENST00000532957.5:n.778G>A
NM_000238.3:c.555G>A , LRG_288t1:c.555G>A	NP_000229.1:p.Ala185=
NM_172056.2:c.555G>A , LRG_288t2:c.555G>A	NP_742053.1:p.Ala185=
XM_011516185.1:c.255G>A	XP_011514487.1:p.Ala85=
XM_011516186.1:c.555G>A	XP_011514488.1:p.Ala185=
XM_011516185.2:c.255G>A	XP_011514487.1:p.Ala85=
XM_011516186.3:c.555G>A	XP_011514488.1:p.Ala185=
XM_017012195.1:c.405G>A	XP_016867684.1:p.Ala135=
XM_017012196.1:c.378G>A	XP_016867685.1:p.Ala126=
NM_000238.4:c.555G>A MANE Select	NP_000229.1:p.Ala185=