Canonical Allele Identifier: CA369863790

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656757G>C (hg19) ; chr7:g.150959669G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959669G>C , CM000669.2:g.150959669G>C	GRCh38
NC_000007.13:g.150656757G>C , CM000669.1:g.150656757G>C	GRCh37
NC_000007.12:g.150287690G>C	NCBI36
NG_008916.1:g.23258C>G , LRG_288:g.23258C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1208C>G
ENST00000262186.10:c.375C>G MANE Select	ENSP00000262186.5:p.Phe125Leu
ENST00000262186.9:c.375C>G	ENSP00000262186.5:p.Phe125Leu
ENST00000430723.4:c.198C>G	ENSP00000387657.4:p.Phe66Leu
ENST00000532957.5:n.598C>G
NM_000238.3:c.375C>G , LRG_288t1:c.375C>G	NP_000229.1:p.Phe125Leu
NM_172056.2:c.375C>G , LRG_288t2:c.375C>G	NP_742053.1:p.Phe125Leu
XM_011516185.1:c.75C>G	XP_011514487.1:p.Phe25Leu
XM_011516186.1:c.375C>G	XP_011514488.1:p.Phe125Leu
XM_011516185.2:c.75C>G	XP_011514487.1:p.Phe25Leu
XM_011516186.3:c.375C>G	XP_011514488.1:p.Phe125Leu
XM_017012195.1:c.225C>G	XP_016867684.1:p.Phe75Leu
XM_017012196.1:c.198C>G	XP_016867685.1:p.Phe66Leu
NM_000238.4:c.375C>G MANE Select	NP_000229.1:p.Phe125Leu