Canonical Allele Identifier: CA1752445556

Gene: KCNH2

Linked Data

• dbSNP Id: rs1563193058

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150977513A>G , CM000669.2:g.150977513A>G	GRCh38
NC_000007.13:g.150674601A>G , CM000669.1:g.150674601A>G	GRCh37
NC_000007.12:g.150305534A>G	NCBI36
NG_008916.1:g.5414T>C , LRG_288:g.5414T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.76+325T>C MANE Select	ENSP00000262186.5:n.76+325T>C
ENST00000262186.9:c.76+325T>C	ENSP00000262186.5:n.76+325T>C
ENST00000430723.4:c.-102+325T>C	ENSP00000387657.4:n.-102+325T>C
ENST00000532957.5:n.299+325T>C
NM_000238.3:c.76+325T>C , LRG_288t1:c.76+325T>C	NP_000229.1:n.76+325T>C
NM_172056.2:c.76+325T>C , LRG_288t2:c.76+325T>C	NP_742053.1:n.76+325T>C
XM_011516186.1:c.76+325T>C	XP_011514488.1:n.76+325T>C
XM_011516186.3:c.76+325T>C	XP_011514488.1:n.76+325T>C
NM_000238.4:c.76+325T>C MANE Select	NP_000229.1:n.76+325T>C