Canonical Allele Identifier: CA2038229329
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041905G= , CM000674.2:g.56041905G= GRCh38
NC_000012.11:g.56435689G= , CM000674.1:g.56435689G= GRCh37
NC_000012.10:g.54721956G= NCBI36
NG_023201.1:g.5004G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-262G= ENSP00000348849.5:n.-262G=
ENST00000356464.9:c.-262G= ENSP00000348849.5:n.-262G=
ENST00000552361.1:c.-194G= ENSP00000450339.1:n.-194G=
NM_001029.3:c.-262G= NP_001020.2:n.-262G=
XR_944989.3:n.99C=
XR_944990.3:n.99C=