Canonical Allele Identifier: CA458645931

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654403G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957315G>A , CM000669.2:g.150957315G>A	GRCh38
NC_000007.13:g.150654403G>A , CM000669.1:g.150654403G>A	GRCh37
NC_000007.12:g.150285336G>A	NCBI36
NG_008916.1:g.25612C>T , LRG_288:g.25612C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1937C>T
ENST00000262186.10:c.1104C>T MANE Select	ENSP00000262186.5:p.His368=
ENST00000262186.9:c.1104C>T	ENSP00000262186.5:p.His368=
ENST00000430723.4:c.756C>T	ENSP00000387657.4:p.His252=
ENST00000532957.5:n.1327C>T
NM_000238.3:c.1104C>T , LRG_288t1:c.1104C>T	NP_000229.1:p.His368=
NM_172056.2:c.1104C>T , LRG_288t2:c.1104C>T	NP_742053.1:p.His368=
XM_011516185.1:c.804C>T	XP_011514487.1:p.His268=
XM_011516186.1:c.1104C>T	XP_011514488.1:p.His368=
XM_011516185.2:c.804C>T	XP_011514487.1:p.His268=
XM_011516186.3:c.1104C>T	XP_011514488.1:p.His368=
XM_017012195.1:c.954C>T	XP_016867684.1:p.His318=
XM_017012196.1:c.927C>T	XP_016867685.1:p.His309=
NM_000238.4:c.1104C>T MANE Select	NP_000229.1:p.His368=