Canonical Allele Identifier: CA835224229

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 2047542
• ClinVar RCV Id: RCV002904384
• dbSNP Id: rs1246466836
• gnomAD v3: 7-150949064-G-A
• gnomAD v4: 7-150949064-G-A
• MyVariant Identifiers: chr7:g.150646152G>A (hg19) ; chr7:g.150949064G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150949064G>A , CM000669.2:g.150949064G>A	GRCh38
NC_000007.13:g.150646152G>A , CM000669.1:g.150646152G>A	GRCh37
NC_000007.12:g.150277085G>A	NCBI36
NG_008916.1:g.33863C>T , LRG_288:g.33863C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3232-15C>T
ENST00000262186.10:c.2399-15C>T MANE Select	ENSP00000262186.5:n.2399-15C>T
ENST00000330883.9:c.1379-15C>T	ENSP00000328531.4:n.1379-15C>T
ENST00000262186.9:c.2399-15C>T	ENSP00000262186.5:n.2399-15C>T
ENST00000330883.8:c.1379-15C>T	ENSP00000328531.4:n.1379-15C>T
NM_000238.3:c.2399-15C>T , LRG_288t1:c.2399-15C>T	NP_000229.1:n.2399-15C>T
NM_172057.2:c.1379-15C>T , LRG_288t3:c.1379-15C>T	NP_742054.1:n.1379-15C>T
XM_011516185.1:c.2099-15C>T	XP_011514487.1:n.2099-15C>T
XM_011516186.1:c.2399-15C>T	XP_011514488.1:n.2399-15C>T
XM_011516185.2:c.2099-15C>T	XP_011514487.1:n.2099-15C>T
XM_011516186.3:c.2399-15C>T	XP_011514488.1:n.2399-15C>T
XM_017012195.1:c.2249-15C>T	XP_016867684.1:n.2249-15C>T
XM_017012196.1:c.2222-15C>T	XP_016867685.1:n.2222-15C>T
NM_000238.4:c.2399-15C>T MANE Select	NP_000229.1:n.2399-15C>T
NM_172057.3:c.1379-15C>T	NP_742054.1:n.1379-15C>T