Canonical Allele Identifier: CA531285385
Gene: KCNS3 HGNC NCBI

Linked Data

dbSNP Id: rs1168066436
gnomAD v2: 2-18114801-C-T
gnomAD v3: 2-17933534-C-T
gnomAD v4: 2-17933534-C-T
MyVariant Identifiers: chr2:g.18114801C>T (hg19) chr2:g.17933534C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17933534C>T , CM000664.2:g.17933534C>T GRCh38
NC_000002.11:g.18114801C>T , CM000664.1:g.18114801C>T GRCh37
NC_000002.10:g.17978282C>T NCBI36
NG_012873.1:g.59857C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465292.5:n.305+15663C>T
Search 100 bp 5'
Search 100 bp 3'