Canonical Allele Identifier: CA458645202

Gene: KCNH2

Linked Data

• dbSNP Id: rs1801032151
• MyVariant Identifiers: chr7:g.150646100A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150949012A>G , CM000669.2:g.150949012A>G	GRCh38
NC_000007.13:g.150646100A>G , CM000669.1:g.150646100A>G	GRCh37
NC_000007.12:g.150277033A>G	NCBI36
NG_008916.1:g.33915T>C , LRG_288:g.33915T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3269T>C
ENST00000262186.10:c.2436T>C MANE Select	ENSP00000262186.5:p.Tyr812=
ENST00000330883.9:c.1416T>C	ENSP00000328531.4:p.Tyr472=
ENST00000262186.9:c.2436T>C	ENSP00000262186.5:p.Tyr812=
ENST00000330883.8:c.1416T>C	ENSP00000328531.4:p.Tyr472=
NM_000238.3:c.2436T>C , LRG_288t1:c.2436T>C	NP_000229.1:p.Tyr812=
NM_172057.2:c.1416T>C , LRG_288t3:c.1416T>C	NP_742054.1:p.Tyr472=
XM_011516185.1:c.2136T>C	XP_011514487.1:p.Tyr712=
XM_011516186.1:c.2436T>C	XP_011514488.1:p.Tyr812=
XM_011516185.2:c.2136T>C	XP_011514487.1:p.Tyr712=
XM_011516186.3:c.2436T>C	XP_011514488.1:p.Tyr812=
XM_017012195.1:c.2286T>C	XP_016867684.1:p.Tyr762=
XM_017012196.1:c.2259T>C	XP_016867685.1:p.Tyr753=
NM_000238.4:c.2436T>C MANE Select	NP_000229.1:p.Tyr812=
NM_172057.3:c.1416T>C	NP_742054.1:p.Tyr472=