Canonical Allele Identifier: CA2038229299
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041880C= , CM000674.2:g.56041880C= GRCh38
NC_000012.11:g.56435664C= , CM000674.1:g.56435664C= GRCh37
NC_000012.10:g.54721931C= NCBI36
NG_023201.1:g.4979C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-287C= ENSP00000348849.5:n.-287C=
ENST00000356464.9:c.-287C= ENSP00000348849.5:n.-287C=
XR_944989.3:n.124G=
XR_944990.3:n.124G=