Canonical Allele Identifier: CA369854759

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 629380
• ClinVar RCV Id: RCV001841923
• dbSNP Id: rs1563150352
• MyVariant Identifiers: chr7:g.150645970G>C (hg19) ; chr7:g.150948882G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948882G>C , CM000669.2:g.150948882G>C	GRCh38
NC_000007.13:g.150645970G>C , CM000669.1:g.150645970G>C	GRCh37
NC_000007.12:g.150276903G>C	NCBI36
NG_008916.1:g.34045C>G , LRG_288:g.34045C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3399C>G
ENST00000262186.10:c.2566C>G MANE Select	ENSP00000262186.5:p.Leu856Val
ENST00000330883.9:c.1546C>G	ENSP00000328531.4:p.Leu516Val
ENST00000262186.9:c.2566C>G	ENSP00000262186.5:p.Leu856Val
ENST00000330883.8:c.1546C>G	ENSP00000328531.4:p.Leu516Val
NM_000238.3:c.2566C>G , LRG_288t1:c.2566C>G	NP_000229.1:p.Leu856Val
NM_172057.2:c.1546C>G , LRG_288t3:c.1546C>G	NP_742054.1:p.Leu516Val
XM_011516185.1:c.2266C>G	XP_011514487.1:p.Leu756Val
XM_011516186.1:c.2566C>G	XP_011514488.1:p.Leu856Val
XM_011516185.2:c.2266C>G	XP_011514487.1:p.Leu756Val
XM_011516186.3:c.2566C>G	XP_011514488.1:p.Leu856Val
XM_017012195.1:c.2416C>G	XP_016867684.1:p.Leu806Val
XM_017012196.1:c.2389C>G	XP_016867685.1:p.Leu797Val
NM_000238.4:c.2566C>G MANE Select	NP_000229.1:p.Leu856Val
NM_172057.3:c.1546C>G	NP_742054.1:p.Leu516Val