Canonical Allele Identifier: CA2619258539
Gene: RPS26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041738del , CM000674.2:g.56041738del GRCh38
NC_000012.11:g.56435522del , CM000674.1:g.56435522del GRCh37
NC_000012.10:g.54721789del NCBI36
NG_023201.1:g.4837del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-73del ENSP00000348849.5:n.-356-73del
XR_944989.3:n.267del
XR_944990.3:n.267del