Canonical Allele Identifier: CA1303193882

Gene: KCNH7

Linked Data

• dbSNP Id: rs1686396368

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162380906A>T , CM000664.2:g.162380906A>T	GRCh38
NC_000002.11:g.163237416A>T , CM000664.1:g.163237416A>T	GRCh37
NC_000002.10:g.162945662A>T	NCBI36
NG_041938.1:g.462842T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.2963-885T>A MANE Select	ENSP00000331727.5:n.2963-885T>A
ENST00000332142.9:c.2963-885T>A	ENSP00000331727.5:n.2963-885T>A
ENST00000618399.4:c.2663-885T>A	ENSP00000482818.1:n.2663-885T>A
NM_033272.3:c.2963-885T>A	NP_150375.2:n.2963-885T>A
XM_011512109.1:c.2987-885T>A	XP_011510411.1:n.2987-885T>A
XM_011512109.3:c.2987-885T>A	XP_011510411.1:n.2987-885T>A
XM_017005218.2:c.2978-885T>A	XP_016860707.1:n.2978-885T>A
XM_017005219.2:c.2954-885T>A	XP_016860708.1:n.2954-885T>A
XM_017005220.2:c.2942-885T>A	XP_016860709.1:n.2942-885T>A
NM_033272.4:c.2963-885T>A MANE Select	NP_150375.2:n.2963-885T>A