Canonical Allele Identifier: CA835215565

Gene: KCNH2

Linked Data

• dbSNP Id: rs1360455009
• gnomAD v3: 7-150977275-A-G
• gnomAD v4: 7-150977275-A-G
• MyVariant Identifiers: chr7:g.150674363A>G (hg19) ; chr7:g.150977275A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150977275A>G , CM000669.2:g.150977275A>G	GRCh38
NC_000007.13:g.150674363A>G , CM000669.1:g.150674363A>G	GRCh37
NC_000007.12:g.150305296A>G	NCBI36
NG_008916.1:g.5652T>C , LRG_288:g.5652T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.76+563T>C MANE Select	ENSP00000262186.5:n.76+563T>C
ENST00000262186.9:c.76+563T>C	ENSP00000262186.5:n.76+563T>C
ENST00000430723.4:c.-102+563T>C	ENSP00000387657.4:n.-102+563T>C
ENST00000532957.5:n.299+563T>C
NM_000238.3:c.76+563T>C , LRG_288t1:c.76+563T>C	NP_000229.1:n.76+563T>C
NM_172056.2:c.76+563T>C , LRG_288t2:c.76+563T>C	NP_742053.1:n.76+563T>C
XM_011516186.1:c.76+563T>C	XP_011514488.1:n.76+563T>C
XM_011516186.3:c.76+563T>C	XP_011514488.1:n.76+563T>C
NM_000238.4:c.76+563T>C MANE Select	NP_000229.1:n.76+563T>C