Canonical Allele Identifier: CA835222797

Gene: KCNH2

Linked Data

• dbSNP Id: rs1278410098
• gnomAD v3: 7-150947911-G-A
• gnomAD v4: 7-150947911-G-A
• MyVariant Identifiers: chr7:g.150644999G>A (hg19) ; chr7:g.150947911G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947911G>A , CM000669.2:g.150947911G>A	GRCh38
NC_000007.13:g.150644999G>A , CM000669.1:g.150644999G>A	GRCh37
NC_000007.12:g.150275932G>A	NCBI36
NG_008916.1:g.35016C>T , LRG_288:g.35016C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3526-33C>T
ENST00000262186.10:c.2693-33C>T MANE Select	ENSP00000262186.5:n.2693-33C>T
ENST00000330883.9:c.1673-33C>T	ENSP00000328531.4:n.1673-33C>T
ENST00000262186.9:c.2693-33C>T	ENSP00000262186.5:n.2693-33C>T
ENST00000330883.8:c.1673-33C>T	ENSP00000328531.4:n.1673-33C>T
NM_000238.3:c.2693-33C>T , LRG_288t1:c.2693-33C>T	NP_000229.1:n.2693-33C>T
NM_172057.2:c.1673-33C>T , LRG_288t3:c.1673-33C>T	NP_742054.1:n.1673-33C>T
XM_011516185.1:c.2393-33C>T	XP_011514487.1:n.2393-33C>T
XM_011516186.1:c.2693-220C>T	XP_011514488.1:n.2693-220C>T
XM_011516185.2:c.2393-33C>T	XP_011514487.1:n.2393-33C>T
XM_011516186.3:c.2693-220C>T	XP_011514488.1:n.2693-220C>T
XM_017012195.1:c.2543-33C>T	XP_016867684.1:n.2543-33C>T
XM_017012196.1:c.2516-33C>T	XP_016867685.1:n.2516-33C>T
NM_000238.4:c.2693-33C>T MANE Select	NP_000229.1:n.2693-33C>T
NM_172057.3:c.1673-33C>T	NP_742054.1:n.1673-33C>T