Canonical Allele Identifier: CA2038229348
Gene: RPS26 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041916T= , CM000674.2:g.56041916T= GRCh38
NC_000012.11:g.56435700T= , CM000674.1:g.56435700T= GRCh37
NC_000012.10:g.54721967T= NCBI36
NG_023201.1:g.5015T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-251T= ENSP00000348849.5:n.-251T=
ENST00000356464.9:c.-251T= ENSP00000348849.5:n.-251T=
ENST00000552361.1:c.-183T= ENSP00000450339.1:n.-183T=
NM_001029.3:c.-251T= NP_001020.2:n.-251T=
XR_944989.3:n.88A=
XR_944990.3:n.88A=
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