Canonical Allele Identifier: CA369853958

Gene: KCNH2

Linked Data

• dbSNP Id: rs1303408486
• MyVariant Identifiers: chr7:g.150645627T>A (hg19) ; chr7:g.150948539T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948539T>A , CM000669.2:g.150948539T>A	GRCh38
NC_000007.13:g.150645627T>A , CM000669.1:g.150645627T>A	GRCh37
NC_000007.12:g.150276560T>A	NCBI36
NG_008916.1:g.34388A>T , LRG_288:g.34388A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3430A>T
ENST00000262186.10:c.2597A>T MANE Select	ENSP00000262186.5:p.Asn866Ile
ENST00000330883.9:c.1577A>T	ENSP00000328531.4:p.Asn526Ile
ENST00000262186.9:c.2597A>T	ENSP00000262186.5:p.Asn866Ile
ENST00000330883.8:c.1577A>T	ENSP00000328531.4:p.Asn526Ile
NM_000238.3:c.2597A>T , LRG_288t1:c.2597A>T	NP_000229.1:p.Asn866Ile
NM_172057.2:c.1577A>T , LRG_288t3:c.1577A>T	NP_742054.1:p.Asn526Ile
XM_011516185.1:c.2297A>T	XP_011514487.1:p.Asn766Ile
XM_011516186.1:c.2597A>T	XP_011514488.1:p.Asn866Ile
XM_011516185.2:c.2297A>T	XP_011514487.1:p.Asn766Ile
XM_011516186.3:c.2597A>T	XP_011514488.1:p.Asn866Ile
XM_017012195.1:c.2447A>T	XP_016867684.1:p.Asn816Ile
XM_017012196.1:c.2420A>T	XP_016867685.1:p.Asn807Ile
NM_000238.4:c.2597A>T MANE Select	NP_000229.1:p.Asn866Ile
NM_172057.3:c.1577A>T	NP_742054.1:p.Asn526Ile