Canonical Allele Identifier: CA369852013

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150644008G>T (hg19) ; chr7:g.150946920G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150946920G>T , CM000669.2:g.150946920G>T	GRCh38
NC_000007.13:g.150644008G>T , CM000669.1:g.150644008G>T	GRCh37
NC_000007.12:g.150274941G>T	NCBI36
NG_008916.1:g.36007C>A , LRG_288:g.36007C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.4120C>A
ENST00000262186.10:c.3287C>A MANE Select	ENSP00000262186.5:p.Pro1096His
ENST00000330883.9:c.2267C>A	ENSP00000328531.4:p.Pro756His
ENST00000262186.9:c.3287C>A	ENSP00000262186.5:p.Pro1096His
ENST00000330883.8:c.2267C>A	ENSP00000328531.4:p.Pro756His
NM_000238.3:c.3287C>A , LRG_288t1:c.3287C>A	NP_000229.1:p.Pro1096His
NM_172057.2:c.2267C>A , LRG_288t3:c.2267C>A	NP_742054.1:p.Pro756His
XM_011516185.1:c.2987C>A	XP_011514487.1:p.Pro996His
XM_011516185.2:c.2987C>A	XP_011514487.1:p.Pro996His
XM_017012195.1:c.3137C>A	XP_016867684.1:p.Pro1046His
XM_017012196.1:c.3110C>A	XP_016867685.1:p.Pro1037His
NM_000238.4:c.3287C>A MANE Select	NP_000229.1:p.Pro1096His
NM_172057.3:c.2267C>A	NP_742054.1:p.Pro756His