Canonical Allele Identifier: CA43636735
Gene: KCNS3 HGNC NCBI

Linked Data

dbSNP Id: rs566129402
gnomAD v2: 2-18114933-G-A
gnomAD v3: 2-17933666-G-A
gnomAD v4: 2-17933666-G-A
MyVariant Identifiers: chr2:g.18114933G>A (hg19) chr2:g.17933666G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17933666G>A , CM000664.2:g.17933666G>A GRCh38
NC_000002.11:g.18114933G>A , CM000664.1:g.18114933G>A GRCh37
NC_000002.10:g.17978414G>A NCBI36
NG_012873.1:g.59989G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465292.5:n.305+15795G>A
Search 100 bp 5'
Search 100 bp 3'