Canonical Allele Identifier: CA744846598

Gene: SLC12A5-AS1

Linked Data

• dbSNP Id: rs1432898013
• gnomAD v3: 20-46016567-A-G
• gnomAD v4: 20-46016567-A-G
• MyVariant Identifiers: chr20:g.44645206A>G (hg19) ; chr20:g.46016567A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46016567A>G , CM000682.2:g.46016567A>G	GRCh38
NC_000020.10:g.44645206A>G , CM000682.1:g.44645206A>G	GRCh37
NC_000020.9:g.44078613A>G	NCBI36
NG_011468.1:g.12660A>G

Transcript Alleles

HGVS	Amino-acid Change
NR_147699.1:n.669-1779T>C