Canonical Allele Identifier: CA2038228856
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895879060

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041520C>A , CM000674.2:g.56041520C>A GRCh38
NC_000012.11:g.56435304C>A , CM000674.1:g.56435304C>A GRCh37
NC_000012.10:g.54721571C>A NCBI36
NG_023201.1:g.4619C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+124C>A ENSP00000348849.5:n.-357+124C>A
XR_944989.1:n.193G>T
XR_944990.1:n.193G>T
XR_944989.3:n.484G>T
XR_944990.3:n.484G>T