Canonical Allele Identifier: CA2038229513
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042070T= , CM000674.2:g.56042070T= GRCh38
NC_000012.11:g.56435854T= , CM000674.1:g.56435854T= GRCh37
NC_000012.10:g.54722121T= NCBI36
NG_023201.1:g.5169T=

Transcript Alleles

HGVS Amino-acid change
ENST00000356464.10:c.-97T= ENSP00000348849.5:n.-97T=
ENST00000646449.2:c.-97T= MANE Select ENSP00000496643.1:n.-97T=
ENST00000356464.9:c.-97T= ENSP00000348849.5:n.-97T=
ENST00000552361.1:c.-35+6T= ENSP00000450339.1:n.-35+6T=
NM_001029.3:c.-97T= NP_001020.2:n.-97T=
NM_001029.5:c.-97T= MANE Select NP_001020.2:n.-97T=