Canonical Allele Identifier: CA458646940

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656766G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959678G>C , CM000669.2:g.150959678G>C	GRCh38
NC_000007.13:g.150656766G>C , CM000669.1:g.150656766G>C	GRCh37
NC_000007.12:g.150287699G>C	NCBI36
NG_008916.1:g.23249C>G , LRG_288:g.23249C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1199C>G
ENST00000262186.10:c.366C>G MANE Select	ENSP00000262186.5:p.Val122=
ENST00000262186.9:c.366C>G	ENSP00000262186.5:p.Val122=
ENST00000430723.4:c.189C>G	ENSP00000387657.4:p.Val63=
ENST00000532957.5:n.589C>G
NM_000238.3:c.366C>G , LRG_288t1:c.366C>G	NP_000229.1:p.Val122=
NM_172056.2:c.366C>G , LRG_288t2:c.366C>G	NP_742053.1:p.Val122=
XM_011516185.1:c.66C>G	XP_011514487.1:p.Val22=
XM_011516186.1:c.366C>G	XP_011514488.1:p.Val122=
XM_011516185.2:c.66C>G	XP_011514487.1:p.Val22=
XM_011516186.3:c.366C>G	XP_011514488.1:p.Val122=
XM_017012195.1:c.216C>G	XP_016867684.1:p.Val72=
XM_017012196.1:c.189C>G	XP_016867685.1:p.Val63=
NM_000238.4:c.366C>G MANE Select	NP_000229.1:p.Val122=