Canonical Allele Identifier: CA744846644
Gene: SLC12A5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1436076632
gnomAD v3: 20-46016628-A-C
gnomAD v4: 20-46016628-A-C
MyVariant Identifiers: chr20:g.44645267A>C (hg19) chr20:g.46016628A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016628A>C , CM000682.2:g.46016628A>C GRCh38
NC_000020.10:g.44645267A>C , CM000682.1:g.44645267A>C GRCh37
NC_000020.9:g.44078674A>C NCBI36
NG_011468.1:g.12721A>C

Transcript Alleles

HGVS Amino-acid Change
NR_147699.1:n.669-1840T>G
Search 100 bp 5'
Search 100 bp 3'