Canonical Allele Identifier: CA947972668
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895886751

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041880C>A , CM000674.2:g.56041880C>A GRCh38
NC_000012.11:g.56435664C>A , CM000674.1:g.56435664C>A GRCh37
NC_000012.10:g.54721931C>A NCBI36
NG_023201.1:g.4979C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-287C>A ENSP00000348849.5:n.-287C>A
ENST00000356464.9:c.-287C>A ENSP00000348849.5:n.-287C>A
XR_944989.3:n.124G>T
XR_944990.3:n.124G>T