Canonical Allele Identifier: CA2619258781
Gene: RPS26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041907C>A , CM000674.2:g.56041907C>A GRCh38
NC_000012.11:g.56435691C>A , CM000674.1:g.56435691C>A GRCh37
NC_000012.10:g.54721958C>A NCBI36
NG_023201.1:g.5006C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-260C>A ENSP00000348849.5:n.-260C>A
ENST00000356464.9:c.-260C>A ENSP00000348849.5:n.-260C>A
ENST00000552361.1:c.-192C>A ENSP00000450339.1:n.-192C>A
NM_001029.3:c.-260C>A NP_001020.2:n.-260C>A
XR_944989.3:n.97G>T
XR_944990.3:n.97G>T