Canonical Allele Identifier: CA169082347

Gene: KCNH2

Linked Data

• dbSNP Id: rs868631953
• MyVariant Identifiers: chr7:g.150656893G>A (hg19) ; chr7:g.150959805G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959805G>A , CM000669.2:g.150959805G>A	GRCh38
NC_000007.13:g.150656893G>A , CM000669.1:g.150656893G>A	GRCh37
NC_000007.12:g.150287826G>A	NCBI36
NG_008916.1:g.23122C>T , LRG_288:g.23122C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1072C>T
ENST00000262186.10:c.308-69C>T MANE Select	ENSP00000262186.5:n.308-69C>T
ENST00000262186.9:c.308-69C>T	ENSP00000262186.5:n.308-69C>T
ENST00000430723.4:c.131-69C>T	ENSP00000387657.4:n.131-69C>T
ENST00000532957.5:n.531-69C>T
NM_000238.3:c.308-69C>T , LRG_288t1:c.308-69C>T	NP_000229.1:n.308-69C>T
NM_172056.2:c.308-69C>T , LRG_288t2:c.308-69C>T	NP_742053.1:n.308-69C>T
XM_011516185.1:c.8-69C>T	XP_011514487.1:n.8-69C>T
XM_011516186.1:c.308-69C>T	XP_011514488.1:n.308-69C>T
XM_011516185.2:c.8-69C>T	XP_011514487.1:n.8-69C>T
XM_011516186.3:c.308-69C>T	XP_011514488.1:n.308-69C>T
XM_017012195.1:c.158-69C>T	XP_016867684.1:n.158-69C>T
XM_017012196.1:c.131-69C>T	XP_016867685.1:n.131-69C>T
NM_000238.4:c.308-69C>T MANE Select	NP_000229.1:n.308-69C>T