Canonical Allele Identifier: CA690167207
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1435738674

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041724_56041730dup , CM000674.2:g.56041724_56041730dup GRCh38
NC_000012.11:g.56435508_56435514dup , CM000674.1:g.56435508_56435514dup GRCh37
NC_000012.10:g.54721775_54721781dup NCBI36
NG_023201.1:g.4823_4829dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-87_-356-81dup ENSP00000348849.5:n.-356-87_-356-81dup
XR_944989.3:n.282_288dup
XR_944990.3:n.282_288dup