Canonical Allele Identifier: CA2038229009
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041676A= , CM000674.2:g.56041676A= GRCh38
NC_000012.11:g.56435460A= , CM000674.1:g.56435460A= GRCh37
NC_000012.10:g.54721727A= NCBI36
NG_023201.1:g.4775A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-135A= ENSP00000348849.5:n.-356-135A=
XR_944989.1:n.37T=
XR_944990.1:n.37T=
XR_944989.3:n.328T=
XR_944990.3:n.328T=