Canonical Allele Identifier: CA16609735

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 402998
• ClinVar RCV Id: RCV000456102 ; RCV000768000 ; RCV002467801 ; RCV001841341 ; RCV001856798
• dbSNP Id: rs906562788
• gnomAD v2: 7-150645941-C-T
• gnomAD v4: 7-150948853-C-T
• MyVariant Identifiers: chr7:g.150645941C>T (hg19) ; chr7:g.150948853C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948853C>T , CM000669.2:g.150948853C>T	GRCh38
NC_000007.13:g.150645941C>T , CM000669.1:g.150645941C>T	GRCh37
NC_000007.12:g.150276874C>T	NCBI36
NG_008916.1:g.34074G>A , LRG_288:g.34074G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3425+3G>A
ENST00000262186.10:c.2592+3G>A MANE Select	ENSP00000262186.5:n.2592+3G>A
ENST00000330883.9:c.1572+3G>A	ENSP00000328531.4:n.1572+3G>A
ENST00000262186.9:c.2592+3G>A	ENSP00000262186.5:n.2592+3G>A
ENST00000330883.8:c.1572+3G>A	ENSP00000328531.4:n.1572+3G>A
NM_000238.3:c.2592+3G>A , LRG_288t1:c.2592+3G>A	NP_000229.1:n.2592+3G>A
NM_172057.2:c.1572+3G>A , LRG_288t3:c.1572+3G>A	NP_742054.1:n.1572+3G>A
XM_011516185.1:c.2292+3G>A	XP_011514487.1:n.2292+3G>A
XM_011516186.1:c.2592+3G>A	XP_011514488.1:n.2592+3G>A
XM_011516185.2:c.2292+3G>A	XP_011514487.1:n.2292+3G>A
XM_011516186.3:c.2592+3G>A	XP_011514488.1:n.2592+3G>A
XM_017012195.1:c.2442+3G>A	XP_016867684.1:n.2442+3G>A
XM_017012196.1:c.2415+3G>A	XP_016867685.1:n.2415+3G>A
NM_000238.4:c.2592+3G>A MANE Select	NP_000229.1:n.2592+3G>A
NM_172057.3:c.1572+3G>A	NP_742054.1:n.1572+3G>A