Allele Registry

Canonical Allele Identifier: CA11059271

Gene: KCNS3 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr2:g.18359378A>G

GRCh37 chr2:g.18540644A>G

Linked Data - Sequence & Population

gnomAD v2:

2:18540644 A / G

gnomAD v3:

2:18359378 A / G

gnomAD v4:

chr2-18359378-A-G

Joint Max Group AF 0.4238239 (NFE)

Genomes Max Group AF 0.4238239 (NFE)

Linked Data - NCBI & NCI

dbSNP:

7580332

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.18359378A>G , CM000664.2:g.18359378A>G	GRCh38
NC_000002.11:g.18540644A>G , CM000664.1:g.18540644A>G	GRCh37
NC_000002.10:g.18404125A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465292.5:n.536-2189A>G

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