Canonical Allele Identifier: CA947972420
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895882725

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041714del , CM000674.2:g.56041714del GRCh38
NC_000012.11:g.56435498del , CM000674.1:g.56435498del GRCh37
NC_000012.10:g.54721765del NCBI36
NG_023201.1:g.4813del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-97del ENSP00000348849.5:n.-356-97del
XR_944989.3:n.291del
XR_944990.3:n.291del