Canonical Allele Identifier: CA531285384
Gene: KCNS3 HGNC NCBI

Linked Data

dbSNP Id: rs1370828666
gnomAD v2: 2-18114778-T-C
gnomAD v3: 2-17933511-T-C
gnomAD v4: 2-17933511-T-C
MyVariant Identifiers: chr2:g.18114778T>C (hg19) chr2:g.17933511T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17933511T>C , CM000664.2:g.17933511T>C GRCh38
NC_000002.11:g.18114778T>C , CM000664.1:g.18114778T>C GRCh37
NC_000002.10:g.17978259T>C NCBI36
NG_012873.1:g.59834T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465292.5:n.305+15640T>C
Search 100 bp 5'
Search 100 bp 3'