Canonical Allele Identifier: CA369853783

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 1510422
• ClinVar RCV Id: RCV002043051
• dbSNP Id: rs2116938251
• MyVariant Identifiers: chr7:g.150645588C>T (hg19) ; chr7:g.150948500C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948500C>T , CM000669.2:g.150948500C>T	GRCh38
NC_000007.13:g.150645588C>T , CM000669.1:g.150645588C>T	GRCh37
NC_000007.12:g.150276521C>T	NCBI36
NG_008916.1:g.34427G>A , LRG_288:g.34427G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3469G>A
ENST00000262186.10:c.2636G>A MANE Select	ENSP00000262186.5:p.Gly879Asp
ENST00000330883.9:c.1616G>A	ENSP00000328531.4:p.Gly539Asp
ENST00000262186.9:c.2636G>A	ENSP00000262186.5:p.Gly879Asp
ENST00000330883.8:c.1616G>A	ENSP00000328531.4:p.Gly539Asp
NM_000238.3:c.2636G>A , LRG_288t1:c.2636G>A	NP_000229.1:p.Gly879Asp
NM_172057.2:c.1616G>A , LRG_288t3:c.1616G>A	NP_742054.1:p.Gly539Asp
XM_011516185.1:c.2336G>A	XP_011514487.1:p.Gly779Asp
XM_011516186.1:c.2636G>A	XP_011514488.1:p.Gly879Asp
XM_011516185.2:c.2336G>A	XP_011514487.1:p.Gly779Asp
XM_011516186.3:c.2636G>A	XP_011514488.1:p.Gly879Asp
XM_017012195.1:c.2486G>A	XP_016867684.1:p.Gly829Asp
XM_017012196.1:c.2459G>A	XP_016867685.1:p.Gly820Asp
NM_000238.4:c.2636G>A MANE Select	NP_000229.1:p.Gly879Asp
NM_172057.3:c.1616G>A	NP_742054.1:p.Gly539Asp