Canonical Allele Identifier: CA10856116
Gene: SLC26A9-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205945629A>G , CM000663.2:g.205945629A>G GRCh38
NC_000001.10:g.205914757A>G , CM000663.1:g.205914757A>G GRCh37
NC_000001.9:g.204181380A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110983.1:n.229+9862A>G
NR_110984.1:n.201+9862A>G