Canonical Allele Identifier: CA761346963

Gene: KCNS3

Linked Data

• dbSNP Id: rs1168220449
• gnomAD v3: 2-17933535-A-C
• gnomAD v4: 2-17933535-A-C
• MyVariant Identifiers: chr2:g.18114802A>C (hg19) ; chr2:g.17933535A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.17933535A>C , CM000664.2:g.17933535A>C	GRCh38
NC_000002.11:g.18114802A>C , CM000664.1:g.18114802A>C	GRCh37
NC_000002.10:g.17978283A>C	NCBI36
NG_012873.1:g.59858A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000465292.5:n.305+15664A>C