Canonical Allele Identifier: CA2038229277
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041866A= , CM000674.2:g.56041866A= GRCh38
NC_000012.11:g.56435650A= , CM000674.1:g.56435650A= GRCh37
NC_000012.10:g.54721917A= NCBI36
NG_023201.1:g.4965A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-301A= ENSP00000348849.5:n.-301A=
ENST00000356464.9:c.-301A= ENSP00000348849.5:n.-301A=
XR_944989.3:n.138T=
XR_944990.3:n.138T=