Canonical Allele Identifier: CA2619258813
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56041935-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041935C>T , CM000674.2:g.56041935C>T GRCh38
NC_000012.11:g.56435719C>T , CM000674.1:g.56435719C>T GRCh37
NC_000012.10:g.54721986C>T NCBI36
NG_023201.1:g.5034C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-232C>T ENSP00000348849.5:n.-232C>T
ENST00000646449.2:c.-232C>T MANE Select ENSP00000496643.1:n.-232C>T
ENST00000356464.9:c.-232C>T ENSP00000348849.5:n.-232C>T
ENST00000552361.1:c.-164C>T ENSP00000450339.1:n.-164C>T
NM_001029.3:c.-232C>T NP_001020.2:n.-232C>T
NM_001029.5:c.-232C>T MANE Select NP_001020.2:n.-232C>T
XR_944989.3:n.69G>A
XR_944990.3:n.69G>A
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