Canonical Allele Identifier: CA2619258965
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56042034-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042034T>G , CM000674.2:g.56042034T>G GRCh38
NC_000012.11:g.56435818T>G , CM000674.1:g.56435818T>G GRCh37
NC_000012.10:g.54722085T>G NCBI36
NG_023201.1:g.5133T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-133T>G ENSP00000348849.5:n.-133T>G
ENST00000646449.2:c.-133T>G MANE Select ENSP00000496643.1:n.-133T>G
ENST00000356464.9:c.-133T>G ENSP00000348849.5:n.-133T>G
ENST00000552361.1:c.-65T>G ENSP00000450339.1:n.-65T>G
NM_001029.3:c.-133T>G NP_001020.2:n.-133T>G
NM_001029.5:c.-133T>G MANE Select NP_001020.2:n.-133T>G
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