Canonical Allele Identifier: CA947972294
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs887755633

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041598C>G , CM000674.2:g.56041598C>G GRCh38
NC_000012.11:g.56435382C>G , CM000674.1:g.56435382C>G GRCh37
NC_000012.10:g.54721649C>G NCBI36
NG_023201.1:g.4697C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+202C>G ENSP00000348849.5:n.-357+202C>G
XR_944989.1:n.115G>C
XR_944990.1:n.115G>C
XR_944989.3:n.406G>C
XR_944990.3:n.406G>C