Canonical Allele Identifier: CA43636680
Gene: KCNS3 HGNC NCBI

Linked Data

dbSNP Id: rs1017924287
gnomAD v2: 2-18114893-A-G
gnomAD v3: 2-17933626-A-G
gnomAD v4: 2-17933626-A-G
MyVariant Identifiers: chr2:g.18114893A>G (hg19) chr2:g.17933626A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17933626A>G , CM000664.2:g.17933626A>G GRCh38
NC_000002.11:g.18114893A>G , CM000664.1:g.18114893A>G GRCh37
NC_000002.10:g.17978374A>G NCBI36
NG_012873.1:g.59949A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000465292.5:n.305+15755A>G
Search 100 bp 5'
Search 100 bp 3'