Canonical Allele Identifier: CA369862981

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150655416G>C (hg19) ; chr7:g.150958328G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958328G>C , CM000669.2:g.150958328G>C	GRCh38
NC_000007.13:g.150655416G>C , CM000669.1:g.150655416G>C	GRCh37
NC_000007.12:g.150286349G>C	NCBI36
NG_008916.1:g.24599C>G , LRG_288:g.24599C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1480C>G
ENST00000262186.10:c.647C>G MANE Select	ENSP00000262186.5:p.Thr216Arg
ENST00000262186.9:c.647C>G	ENSP00000262186.5:p.Thr216Arg
ENST00000430723.4:c.299C>G	ENSP00000387657.4:p.Thr100Arg
ENST00000532957.5:n.870C>G
NM_000238.3:c.647C>G , LRG_288t1:c.647C>G	NP_000229.1:p.Thr216Arg
NM_172056.2:c.647C>G , LRG_288t2:c.647C>G	NP_742053.1:p.Thr216Arg
XM_011516185.1:c.347C>G	XP_011514487.1:p.Thr116Arg
XM_011516186.1:c.647C>G	XP_011514488.1:p.Thr216Arg
XM_011516185.2:c.347C>G	XP_011514487.1:p.Thr116Arg
XM_011516186.3:c.647C>G	XP_011514488.1:p.Thr216Arg
XM_017012195.1:c.497C>G	XP_016867684.1:p.Thr166Arg
XM_017012196.1:c.470C>G	XP_016867685.1:p.Thr157Arg
NM_000238.4:c.647C>G MANE Select	NP_000229.1:p.Thr216Arg