Canonical Allele Identifier: CA1140010517
Gene: SLC26A9-AS1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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