Canonical Allele Identifier: CA369862302

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 1978071
• ClinVar RCV Id: RCV002774963
• MyVariant Identifiers: chr7:g.150655227A>C (hg19) ; chr7:g.150958139A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958139A>C , CM000669.2:g.150958139A>C	GRCh38
NC_000007.13:g.150655227A>C , CM000669.1:g.150655227A>C	GRCh37
NC_000007.12:g.150286160A>C	NCBI36
NG_008916.1:g.24788T>G , LRG_288:g.24788T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1669T>G
ENST00000262186.10:c.836T>G MANE Select	ENSP00000262186.5:p.Val279Gly
ENST00000262186.9:c.836T>G	ENSP00000262186.5:p.Val279Gly
ENST00000430723.4:c.488T>G	ENSP00000387657.4:p.Val163Gly
ENST00000532957.5:n.1059T>G
NM_000238.3:c.836T>G , LRG_288t1:c.836T>G	NP_000229.1:p.Val279Gly
NM_172056.2:c.836T>G , LRG_288t2:c.836T>G	NP_742053.1:p.Val279Gly
XM_011516185.1:c.536T>G	XP_011514487.1:p.Val179Gly
XM_011516186.1:c.836T>G	XP_011514488.1:p.Val279Gly
XM_011516185.2:c.536T>G	XP_011514487.1:p.Val179Gly
XM_011516186.3:c.836T>G	XP_011514488.1:p.Val279Gly
XM_017012195.1:c.686T>G	XP_016867684.1:p.Val229Gly
XM_017012196.1:c.659T>G	XP_016867685.1:p.Val220Gly
NM_000238.4:c.836T>G MANE Select	NP_000229.1:p.Val279Gly