Canonical Allele Identifier: CA59694058

Gene: KCNH7

Linked Data

• dbSNP Id: rs776590802
• gnomAD v3: 2-162380798-C-T
• gnomAD v4: 2-162380798-C-T
• MyVariant Identifiers: chr2:g.163237308C>T (hg19) ; chr2:g.162380798C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162380798C>T , CM000664.2:g.162380798C>T	GRCh38
NC_000002.11:g.163237308C>T , CM000664.1:g.163237308C>T	GRCh37
NC_000002.10:g.162945554C>T	NCBI36
NG_041938.1:g.462950G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332142.10:c.2963-777G>A MANE Select	ENSP00000331727.5:n.2963-777G>A
ENST00000332142.9:c.2963-777G>A	ENSP00000331727.5:n.2963-777G>A
ENST00000618399.4:c.2663-777G>A	ENSP00000482818.1:n.2663-777G>A
NM_033272.3:c.2963-777G>A	NP_150375.2:n.2963-777G>A
XM_011512109.1:c.2987-777G>A	XP_011510411.1:n.2987-777G>A
XM_011512109.3:c.2987-777G>A	XP_011510411.1:n.2987-777G>A
XM_017005218.2:c.2978-777G>A	XP_016860707.1:n.2978-777G>A
XM_017005219.2:c.2954-777G>A	XP_016860708.1:n.2954-777G>A
XM_017005220.2:c.2942-777G>A	XP_016860709.1:n.2942-777G>A
NM_033272.4:c.2963-777G>A MANE Select	NP_150375.2:n.2963-777G>A