Canonical Allele Identifier: CA2038229568
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895891583
gnomAD v4: 12-56042126-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042126C>T , CM000674.2:g.56042126C>T GRCh38
NC_000012.11:g.56435910C>T , CM000674.1:g.56435910C>T GRCh37
NC_000012.10:g.54722177C>T NCBI36
NG_023201.1:g.5225C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-41C>T ENSP00000348849.5:n.-41C>T
ENST00000646449.2:c.-41C>T MANE Select ENSP00000496643.1:n.-41C>T
ENST00000356464.9:c.-41C>T ENSP00000348849.5:n.-41C>T
ENST00000552361.1:c.-34-7C>T ENSP00000450339.1:n.-34-7C>T
NM_001029.3:c.-41C>T NP_001020.2:n.-41C>T
NM_001029.5:c.-41C>T MANE Select NP_001020.2:n.-41C>T
Search 100 bp 5'
Search 100 bp 3'