Canonical Allele Identifier: CA2685605952

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150975074-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150975074T>G , CM000669.2:g.150975074T>G	GRCh38
NC_000007.13:g.150672162T>G , CM000669.1:g.150672162T>G	GRCh37
NC_000007.12:g.150303095T>G	NCBI36
NG_008916.1:g.7853A>C , LRG_288:g.7853A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.77-133A>C MANE Select	ENSP00000262186.5:n.77-133A>C
ENST00000262186.9:c.77-133A>C	ENSP00000262186.5:n.77-133A>C
ENST00000430723.4:c.-101-133A>C	ENSP00000387657.4:n.-101-133A>C
ENST00000532957.5:n.300-133A>C
NM_000238.3:c.77-133A>C , LRG_288t1:c.77-133A>C	NP_000229.1:n.77-133A>C
NM_172056.2:c.77-133A>C , LRG_288t2:c.77-133A>C	NP_742053.1:n.77-133A>C
XM_011516186.1:c.77-133A>C	XP_011514488.1:n.77-133A>C
XM_011516186.3:c.77-133A>C	XP_011514488.1:n.77-133A>C
NM_000238.4:c.77-133A>C MANE Select	NP_000229.1:n.77-133A>C