Canonical Allele Identifier: CA43636532

Gene: KCNS3

Linked Data

• dbSNP Id: rs967617011
• MyVariant Identifiers: chr2:g.18114772T>C (hg19) ; chr2:g.17933505T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.17933505T>C , CM000664.2:g.17933505T>C	GRCh38
NC_000002.11:g.18114772T>C , CM000664.1:g.18114772T>C	GRCh37
NC_000002.10:g.17978253T>C	NCBI36
NG_012873.1:g.59828T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465292.5:n.305+15634T>C