Canonical Allele Identifier: CA744846622
Gene: SLC12A5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1247976426
gnomAD v4: 20-46016620-T-C
MyVariant Identifiers: chr20:g.44645259T>C (hg19) chr20:g.46016620T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016620T>C , CM000682.2:g.46016620T>C GRCh38
NC_000020.10:g.44645259T>C , CM000682.1:g.44645259T>C GRCh37
NC_000020.9:g.44078666T>C NCBI36
NG_011468.1:g.12713T>C

Transcript Alleles

HGVS Amino-acid Change
NR_147699.1:n.669-1832A>G
Search 100 bp 5'
Search 100 bp 3'