Canonical Allele Identifier: CA2038229556
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895891420
gnomAD v4: 12-56042122-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042122G>A , CM000674.2:g.56042122G>A GRCh38
NC_000012.11:g.56435906G>A , CM000674.1:g.56435906G>A GRCh37
NC_000012.10:g.54722173G>A NCBI36
NG_023201.1:g.5221G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-45G>A ENSP00000348849.5:n.-45G>A
ENST00000646449.2:c.-45G>A MANE Select ENSP00000496643.1:n.-45G>A
ENST00000356464.9:c.-45G>A ENSP00000348849.5:n.-45G>A
ENST00000552361.1:c.-34-11G>A ENSP00000450339.1:n.-34-11G>A
NM_001029.3:c.-45G>A NP_001020.2:n.-45G>A
NM_001029.5:c.-45G>A MANE Select NP_001020.2:n.-45G>A
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