Canonical Allele Identifier: CA2038228928
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041598C= , CM000674.2:g.56041598C= GRCh38
NC_000012.11:g.56435382C= , CM000674.1:g.56435382C= GRCh37
NC_000012.10:g.54721649C= NCBI36
NG_023201.1:g.4697C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+202C= ENSP00000348849.5:n.-357+202C=
XR_944989.1:n.115G=
XR_944990.1:n.115G=
XR_944989.3:n.406G=
XR_944990.3:n.406G=