Canonical Allele Identifier: CA006261

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 67366
• ClinVar RCV Id: RCV000058086 ; RCV000181935 ; RCV001194446
• dbSNP Id: rs199473420
• MyVariant Identifiers: chr7:g.150671895C>G (hg19) ; chr7:g.150974807C>G (hg38)
• PubMed: PMID:16414944 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974807C>G , CM000669.2:g.150974807C>G	GRCh38
NC_000007.13:g.150671895C>G , CM000669.1:g.150671895C>G	GRCh37
NC_000007.12:g.150302828C>G	NCBI36
NG_008916.1:g.8120G>C , LRG_288:g.8120G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.211G>C MANE Select	ENSP00000262186.5:p.Gly71Arg
ENST00000262186.9:c.211G>C	ENSP00000262186.5:p.Gly71Arg
ENST00000430723.4:c.34G>C	ENSP00000387657.4:p.Gly12Arg
ENST00000532957.5:n.434G>C
NM_000238.3:c.211G>C , LRG_288t1:c.211G>C	NP_000229.1:p.Gly71Arg
NM_172056.2:c.211G>C , LRG_288t2:c.211G>C	NP_742053.1:p.Gly71Arg
XM_011516186.1:c.211G>C	XP_011514488.1:p.Gly71Arg
XM_011516186.3:c.211G>C	XP_011514488.1:p.Gly71Arg
XM_017012196.1:c.34G>C	XP_016867685.1:p.Gly12Arg
NM_000238.4:c.211G>C MANE Select	NP_000229.1:p.Gly71Arg