Canonical Allele Identifier: CA947972307
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1309853570

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041620C>G , CM000674.2:g.56041620C>G GRCh38
NC_000012.11:g.56435404C>G , CM000674.1:g.56435404C>G GRCh37
NC_000012.10:g.54721671C>G NCBI36
NG_023201.1:g.4719C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-191C>G ENSP00000348849.5:n.-356-191C>G
XR_944989.1:n.93G>C
XR_944990.1:n.93G>C
XR_944989.3:n.384G>C
XR_944990.3:n.384G>C