Canonical Allele Identifier: CA2038228968
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041633A= , CM000674.2:g.56041633A= GRCh38
NC_000012.11:g.56435417A= , CM000674.1:g.56435417A= GRCh37
NC_000012.10:g.54721684A= NCBI36
NG_023201.1:g.4732A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-178A= ENSP00000348849.5:n.-356-178A=
XR_944989.1:n.80T=
XR_944990.1:n.80T=
XR_944989.3:n.371T=
XR_944990.3:n.371T=