Canonical Allele Identifier: CA369853260

Gene: KCNH2

Linked Data

• dbSNP Id: rs753735368
• gnomAD v2: 7-150644805-G-T
• gnomAD v4: 7-150947717-G-T
• MyVariant Identifiers: chr7:g.150644805G>T (hg19) ; chr7:g.150947717G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947717G>T , CM000669.2:g.150947717G>T	GRCh38
NC_000007.13:g.150644805G>T , CM000669.1:g.150644805G>T	GRCh37
NC_000007.12:g.150275738G>T	NCBI36
NG_008916.1:g.35210C>A , LRG_288:g.35210C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3687C>A
ENST00000262186.10:c.2854C>A MANE Select	ENSP00000262186.5:p.Pro952Thr
ENST00000330883.9:c.1834C>A	ENSP00000328531.4:p.Pro612Thr
ENST00000262186.9:c.2854C>A	ENSP00000262186.5:p.Pro952Thr
ENST00000330883.8:c.1834C>A	ENSP00000328531.4:p.Pro612Thr
NM_000238.3:c.2854C>A , LRG_288t1:c.2854C>A	NP_000229.1:p.Pro952Thr
NM_172057.2:c.1834C>A , LRG_288t3:c.1834C>A	NP_742054.1:p.Pro612Thr
XM_011516185.1:c.2554C>A	XP_011514487.1:p.Pro852Thr
XM_011516186.1:c.2693-26C>A	XP_011514488.1:n.2693-26C>A
XM_011516185.2:c.2554C>A	XP_011514487.1:p.Pro852Thr
XM_011516186.3:c.2693-26C>A	XP_011514488.1:n.2693-26C>A
XM_017012195.1:c.2704C>A	XP_016867684.1:p.Pro902Thr
XM_017012196.1:c.2677C>A	XP_016867685.1:p.Pro893Thr
NM_000238.4:c.2854C>A MANE Select	NP_000229.1:p.Pro952Thr
NM_172057.3:c.1834C>A	NP_742054.1:p.Pro612Thr