Canonical Allele Identifier: CA169071933

Gene: KCNH2

Linked Data

• dbSNP Id: rs78976657
• gnomAD v4: 7-150947392-G-A
• MyVariant Identifiers: chr7:g.150644480G>A (hg19) ; chr7:g.150947392G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947392G>A , CM000669.2:g.150947392G>A	GRCh38
NC_000007.13:g.150644480G>A , CM000669.1:g.150644480G>A	GRCh37
NC_000007.12:g.150275413G>A	NCBI36
NG_008916.1:g.35535C>T , LRG_288:g.35535C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3921C>T
ENST00000262186.10:c.3088C>T MANE Select	ENSP00000262186.5:p.Pro1030Ser
ENST00000330883.9:c.2068C>T	ENSP00000328531.4:p.Pro690Ser
ENST00000262186.9:c.3088C>T	ENSP00000262186.5:p.Pro1030Ser
ENST00000330883.8:c.2068C>T	ENSP00000328531.4:p.Pro690Ser
NM_000238.3:c.3088C>T , LRG_288t1:c.3088C>T	NP_000229.1:p.Pro1030Ser
NM_172057.2:c.2068C>T , LRG_288t3:c.2068C>T	NP_742054.1:p.Pro690Ser
XM_011516185.1:c.2788C>T	XP_011514487.1:p.Pro930Ser
XM_011516185.2:c.2788C>T	XP_011514487.1:p.Pro930Ser
XM_017012195.1:c.2938C>T	XP_016867684.1:p.Pro980Ser
XM_017012196.1:c.2911C>T	XP_016867685.1:p.Pro971Ser
NM_000238.4:c.3088C>T MANE Select	NP_000229.1:p.Pro1030Ser
NM_172057.3:c.2068C>T	NP_742054.1:p.Pro690Ser