Canonical Allele Identifier: CA369863054

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958349-G-T
• MyVariant Identifiers: chr7:g.150655437G>T (hg19) ; chr7:g.150958349G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958349G>T , CM000669.2:g.150958349G>T	GRCh38
NC_000007.13:g.150655437G>T , CM000669.1:g.150655437G>T	GRCh37
NC_000007.12:g.150286370G>T	NCBI36
NG_008916.1:g.24578C>A , LRG_288:g.24578C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1459C>A
ENST00000262186.10:c.626C>A MANE Select	ENSP00000262186.5:p.Ser209Ter
ENST00000262186.9:c.626C>A	ENSP00000262186.5:p.Ser209Ter
ENST00000430723.4:c.278C>A	ENSP00000387657.4:p.Ser93Ter
ENST00000532957.5:n.849C>A
NM_000238.3:c.626C>A , LRG_288t1:c.626C>A	NP_000229.1:p.Ser209Ter
NM_172056.2:c.626C>A , LRG_288t2:c.626C>A	NP_742053.1:p.Ser209Ter
XM_011516185.1:c.326C>A	XP_011514487.1:p.Ser109Ter
XM_011516186.1:c.626C>A	XP_011514488.1:p.Ser209Ter
XM_011516185.2:c.326C>A	XP_011514487.1:p.Ser109Ter
XM_011516186.3:c.626C>A	XP_011514488.1:p.Ser209Ter
XM_017012195.1:c.476C>A	XP_016867684.1:p.Ser159Ter
XM_017012196.1:c.449C>A	XP_016867685.1:p.Ser150Ter
NM_000238.4:c.626C>A MANE Select	NP_000229.1:p.Ser209Ter