Canonical Allele Identifier: CA605259168
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1344084282

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041888C>G , CM000674.2:g.56041888C>G GRCh38
NC_000012.11:g.56435672C>G , CM000674.1:g.56435672C>G GRCh37
NC_000012.10:g.54721939C>G NCBI36
NG_023201.1:g.4987C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-279C>G ENSP00000348849.5:n.-279C>G
ENST00000356464.9:c.-279C>G ENSP00000348849.5:n.-279C>G
XR_944989.3:n.116G>C
XR_944990.3:n.116G>C