Canonical Allele Identifier: CA59694334

Gene: KCNH7

Linked Data

• dbSNP Id: rs931261334
• MyVariant Identifiers: chr2:g.163237597T>A (hg19) ; chr2:g.162381087T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162381087T>A , CM000664.2:g.162381087T>A	GRCh38
NC_000002.11:g.163237597T>A , CM000664.1:g.163237597T>A	GRCh37
NC_000002.10:g.162945843T>A	NCBI36
NG_041938.1:g.462661A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.2963-1066A>T MANE Select	ENSP00000331727.5:n.2963-1066A>T
ENST00000332142.9:c.2963-1066A>T	ENSP00000331727.5:n.2963-1066A>T
ENST00000618399.4:c.2663-1066A>T	ENSP00000482818.1:n.2663-1066A>T
NM_033272.3:c.2963-1066A>T	NP_150375.2:n.2963-1066A>T
XM_011512109.1:c.2987-1066A>T	XP_011510411.1:n.2987-1066A>T
XM_011512109.3:c.2987-1066A>T	XP_011510411.1:n.2987-1066A>T
XM_017005218.2:c.2978-1066A>T	XP_016860707.1:n.2978-1066A>T
XM_017005219.2:c.2954-1066A>T	XP_016860708.1:n.2954-1066A>T
XM_017005220.2:c.2942-1066A>T	XP_016860709.1:n.2942-1066A>T
NM_033272.4:c.2963-1066A>T MANE Select	NP_150375.2:n.2963-1066A>T