Canonical Allele Identifier: CA369861463

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150957316-T-G
• MyVariant Identifiers: chr7:g.150654404T>G (hg19) ; chr7:g.150957316T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957316T>G , CM000669.2:g.150957316T>G	GRCh38
NC_000007.13:g.150654404T>G , CM000669.1:g.150654404T>G	GRCh37
NC_000007.12:g.150285337T>G	NCBI36
NG_008916.1:g.25611A>C , LRG_288:g.25611A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1936A>C
ENST00000262186.10:c.1103A>C MANE Select	ENSP00000262186.5:p.His368Pro
ENST00000262186.9:c.1103A>C	ENSP00000262186.5:p.His368Pro
ENST00000430723.4:c.755A>C	ENSP00000387657.4:p.His252Pro
ENST00000532957.5:n.1326A>C
NM_000238.3:c.1103A>C , LRG_288t1:c.1103A>C	NP_000229.1:p.His368Pro
NM_172056.2:c.1103A>C , LRG_288t2:c.1103A>C	NP_742053.1:p.His368Pro
XM_011516185.1:c.803A>C	XP_011514487.1:p.His268Pro
XM_011516186.1:c.1103A>C	XP_011514488.1:p.His368Pro
XM_011516185.2:c.803A>C	XP_011514487.1:p.His268Pro
XM_011516186.3:c.1103A>C	XP_011514488.1:p.His368Pro
XM_017012195.1:c.953A>C	XP_016867684.1:p.His318Pro
XM_017012196.1:c.926A>C	XP_016867685.1:p.His309Pro
NM_000238.4:c.1103A>C MANE Select	NP_000229.1:p.His368Pro