Canonical Allele Identifier: CA2038229318
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041901G= , CM000674.2:g.56041901G= GRCh38
NC_000012.11:g.56435685G= , CM000674.1:g.56435685G= GRCh37
NC_000012.10:g.54721952G= NCBI36
NG_023201.1:g.5000G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-266G= ENSP00000348849.5:n.-266G=
ENST00000356464.9:c.-266G= ENSP00000348849.5:n.-266G=
ENST00000552361.1:c.-198G= ENSP00000450339.1:n.-198G=
XR_944989.3:n.103C=
XR_944990.3:n.103C=