Canonical Allele Identifier: CA315639797

Gene: SLC12A5-AS1

Linked Data

• dbSNP Id: rs868064141
• gnomAD v2: 20-44645269-A-C
• gnomAD v3: 20-46016630-A-C
• gnomAD v4: 20-46016630-A-C
• MyVariant Identifiers: chr20:g.44645269A>C (hg19) ; chr20:g.46016630A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46016630A>C , CM000682.2:g.46016630A>C	GRCh38
NC_000020.10:g.44645269A>C , CM000682.1:g.44645269A>C	GRCh37
NC_000020.9:g.44078676A>C	NCBI36
NG_011468.1:g.12723A>C

Transcript Alleles

HGVS	Amino-acid Change
NR_147699.1:n.669-1842T>G