Canonical Allele Identifier: CA458646029

Gene: KCNH2

Linked Data

• dbSNP Id: rs1412814223
• gnomAD v2: 7-150654505-G-C
• MyVariant Identifiers: chr7:g.150654505G>C (hg19) ; chr7:g.150957417G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957417G>C , CM000669.2:g.150957417G>C	GRCh38
NC_000007.13:g.150654505G>C , CM000669.1:g.150654505G>C	GRCh37
NC_000007.12:g.150285438G>C	NCBI36
NG_008916.1:g.25510C>G , LRG_288:g.25510C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1835C>G
ENST00000262186.10:c.1002C>G MANE Select	ENSP00000262186.5:p.Pro334=
ENST00000262186.9:c.1002C>G	ENSP00000262186.5:p.Pro334=
ENST00000430723.4:c.654C>G	ENSP00000387657.4:p.Pro218=
ENST00000532957.5:n.1225C>G
NM_000238.3:c.1002C>G , LRG_288t1:c.1002C>G	NP_000229.1:p.Pro334=
NM_172056.2:c.1002C>G , LRG_288t2:c.1002C>G	NP_742053.1:p.Pro334=
XM_011516185.1:c.702C>G	XP_011514487.1:p.Pro234=
XM_011516186.1:c.1002C>G	XP_011514488.1:p.Pro334=
XM_011516185.2:c.702C>G	XP_011514487.1:p.Pro234=
XM_011516186.3:c.1002C>G	XP_011514488.1:p.Pro334=
XM_017012195.1:c.852C>G	XP_016867684.1:p.Pro284=
XM_017012196.1:c.825C>G	XP_016867685.1:p.Pro275=
NM_000238.4:c.1002C>G MANE Select	NP_000229.1:p.Pro334=