Canonical Allele Identifier: CA071891

Gene: KCNH2

Linked Data

• dbSNP Id: rs772979825
• gnomAD v2: 7-150655373-C-A
• gnomAD v4: 7-150958285-C-A
• MyVariant Identifiers: chr7:g.150655373C>A (hg19) ; chr7:g.150958285C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958285C>A , CM000669.2:g.150958285C>A	GRCh38
NC_000007.13:g.150655373C>A , CM000669.1:g.150655373C>A	GRCh37
NC_000007.12:g.150286306C>A	NCBI36
NG_008916.1:g.24642G>T , LRG_288:g.24642G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1523G>T
ENST00000262186.10:c.690G>T MANE Select	ENSP00000262186.5:p.Glu230Asp
ENST00000262186.9:c.690G>T	ENSP00000262186.5:p.Glu230Asp
ENST00000430723.4:c.342G>T	ENSP00000387657.4:p.Glu114Asp
ENST00000532957.5:n.913G>T
NM_000238.3:c.690G>T , LRG_288t1:c.690G>T	NP_000229.1:p.Glu230Asp
NM_172056.2:c.690G>T , LRG_288t2:c.690G>T	NP_742053.1:p.Glu230Asp
XM_011516185.1:c.390G>T	XP_011514487.1:p.Glu130Asp
XM_011516186.1:c.690G>T	XP_011514488.1:p.Glu230Asp
XM_011516185.2:c.390G>T	XP_011514487.1:p.Glu130Asp
XM_011516186.3:c.690G>T	XP_011514488.1:p.Glu230Asp
XM_017012195.1:c.540G>T	XP_016867684.1:p.Glu180Asp
XM_017012196.1:c.513G>T	XP_016867685.1:p.Glu171Asp
NM_000238.4:c.690G>T MANE Select	NP_000229.1:p.Glu230Asp