Canonical Allele Identifier: CA458871853

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150655211C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958123C>G , CM000669.2:g.150958123C>G	GRCh38
NC_000007.13:g.150655211C>G , CM000669.1:g.150655211C>G	GRCh37
NC_000007.12:g.150286144C>G	NCBI36
NG_008916.1:g.24804G>C , LRG_288:g.24804G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1685G>C
ENST00000262186.10:c.852G>C MANE Select	ENSP00000262186.5:p.Ser284=
ENST00000262186.9:c.852G>C	ENSP00000262186.5:p.Ser284=
ENST00000430723.4:c.504G>C	ENSP00000387657.4:p.Ser168=
ENST00000532957.5:n.1075G>C
NM_000238.3:c.852G>C , LRG_288t1:c.852G>C	NP_000229.1:p.Ser284=
NM_172056.2:c.852G>C , LRG_288t2:c.852G>C	NP_742053.1:p.Ser284=
XM_011516185.1:c.552G>C	XP_011514487.1:p.Ser184=
XM_011516186.1:c.852G>C	XP_011514488.1:p.Ser284=
XM_011516185.2:c.552G>C	XP_011514487.1:p.Ser184=
XM_011516186.3:c.852G>C	XP_011514488.1:p.Ser284=
XM_017012195.1:c.702G>C	XP_016867684.1:p.Ser234=
XM_017012196.1:c.675G>C	XP_016867685.1:p.Ser225=
NM_000238.4:c.852G>C MANE Select	NP_000229.1:p.Ser284=