Canonical Allele Identifier: CA2619258022
Gene: RPS26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041539T>G , CM000674.2:g.56041539T>G GRCh38
NC_000012.11:g.56435323T>G , CM000674.1:g.56435323T>G GRCh37
NC_000012.10:g.54721590T>G NCBI36
NG_023201.1:g.4638T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+143T>G ENSP00000348849.5:n.-357+143T>G
XR_944989.1:n.174A>C
XR_944990.1:n.174A>C
XR_944989.3:n.465A>C
XR_944990.3:n.465A>C