Canonical Allele Identifier: CA2038228852
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895878981

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041515_56041516del , CM000674.2:g.56041515_56041516del GRCh38
NC_000012.11:g.56435299_56435300del , CM000674.1:g.56435299_56435300del GRCh37
NC_000012.10:g.54721566_54721567del NCBI36
NG_023201.1:g.4614_4615del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+119_-357+120del ENSP00000348849.5:n.-357+119_-357+120del
XR_944989.1:n.198_199del
XR_944990.1:n.198_199del
XR_944989.3:n.489_490del
XR_944990.3:n.489_490del