Canonical Allele Identifier: CA2575186513
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56042069-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042069G>A , CM000674.2:g.56042069G>A GRCh38
NC_000012.11:g.56435853G>A , CM000674.1:g.56435853G>A GRCh37
NC_000012.10:g.54722120G>A NCBI36
NG_023201.1:g.5168G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-98G>A ENSP00000348849.5:n.-98G>A
ENST00000646449.2:c.-98G>A MANE Select ENSP00000496643.1:n.-98G>A
ENST00000356464.9:c.-98G>A ENSP00000348849.5:n.-98G>A
ENST00000552361.1:c.-35+5G>A ENSP00000450339.1:n.-35+5G>A
NM_001029.3:c.-98G>A NP_001020.2:n.-98G>A
NM_001029.5:c.-98G>A MANE Select NP_001020.2:n.-98G>A
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