Canonical Allele Identifier: CA039328

Gene: KCNH2

Linked Data

• dbSNP Id: rs563894982
• ExAC: 7:150656724 G / A
• gnomAD v2: 7-150656724-G-A
• gnomAD v3: 7-150959636-G-A
• gnomAD v4: 7-150959636-G-A
• MyVariant Identifiers: chr7:g.150656724G>A (hg19) ; chr7:g.150959636G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959636G>A , CM000669.2:g.150959636G>A	GRCh38
NC_000007.13:g.150656724G>A , CM000669.1:g.150656724G>A	GRCh37
NC_000007.12:g.150287657G>A	NCBI36
NG_008916.1:g.23291C>T , LRG_288:g.23291C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1241C>T
ENST00000262186.10:c.408C>T MANE Select	ENSP00000262186.5:p.Asp136=
ENST00000262186.9:c.408C>T	ENSP00000262186.5:p.Asp136=
ENST00000430723.4:c.231C>T	ENSP00000387657.4:p.Asp77=
ENST00000532957.5:n.631C>T
NM_000238.3:c.408C>T , LRG_288t1:c.408C>T	NP_000229.1:p.Asp136=
NM_172056.2:c.408C>T , LRG_288t2:c.408C>T	NP_742053.1:p.Asp136=
XM_011516185.1:c.108C>T	XP_011514487.1:p.Asp36=
XM_011516186.1:c.408C>T	XP_011514488.1:p.Asp136=
XM_011516185.2:c.108C>T	XP_011514487.1:p.Asp36=
XM_011516186.3:c.408C>T	XP_011514488.1:p.Asp136=
XM_017012195.1:c.258C>T	XP_016867684.1:p.Asp86=
XM_017012196.1:c.231C>T	XP_016867685.1:p.Asp77=
NM_000238.4:c.408C>T MANE Select	NP_000229.1:p.Asp136=