Canonical Allele Identifier: CA2038228870
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895879391

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041541_56041548del , CM000674.2:g.56041541_56041548del GRCh38
NC_000012.11:g.56435325_56435332del , CM000674.1:g.56435325_56435332del GRCh37
NC_000012.10:g.54721592_54721599del NCBI36
NG_023201.1:g.4640_4647del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+145_-357+152del ENSP00000348849.5:n.-357+145_-357+152del
XR_944989.1:n.168_175del
XR_944990.1:n.168_175del
XR_944989.3:n.459_466del
XR_944990.3:n.459_466del