Canonical Allele Identifier: CA835214398

Gene: KCNH2

Linked Data

• dbSNP Id: rs1485314535
• gnomAD v3: 7-150975119-T-G
• gnomAD v4: 7-150975119-T-G
• MyVariant Identifiers: chr7:g.150672207T>G (hg19) ; chr7:g.150975119T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150975119T>G , CM000669.2:g.150975119T>G	GRCh38
NC_000007.13:g.150672207T>G , CM000669.1:g.150672207T>G	GRCh37
NC_000007.12:g.150303140T>G	NCBI36
NG_008916.1:g.7808A>C , LRG_288:g.7808A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.77-178A>C MANE Select	ENSP00000262186.5:n.77-178A>C
ENST00000262186.9:c.77-178A>C	ENSP00000262186.5:n.77-178A>C
ENST00000430723.4:c.-101-178A>C	ENSP00000387657.4:n.-101-178A>C
ENST00000532957.5:n.300-178A>C
NM_000238.3:c.77-178A>C , LRG_288t1:c.77-178A>C	NP_000229.1:n.77-178A>C
NM_172056.2:c.77-178A>C , LRG_288t2:c.77-178A>C	NP_742053.1:n.77-178A>C
XM_011516186.1:c.77-178A>C	XP_011514488.1:n.77-178A>C
XM_011516186.3:c.77-178A>C	XP_011514488.1:n.77-178A>C
NM_000238.4:c.77-178A>C MANE Select	NP_000229.1:n.77-178A>C