Canonical Allele Identifier: CA2038229351
Gene: RPS26 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041918G= , CM000674.2:g.56041918G= GRCh38
NC_000012.11:g.56435702G= , CM000674.1:g.56435702G= GRCh37
NC_000012.10:g.54721969G= NCBI36
NG_023201.1:g.5017G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-249G= ENSP00000348849.5:n.-249G=
ENST00000646449.2:c.-249G= MANE Select ENSP00000496643.1:n.-249G=
ENST00000356464.9:c.-249G= ENSP00000348849.5:n.-249G=
ENST00000552361.1:c.-181G= ENSP00000450339.1:n.-181G=
NM_001029.3:c.-249G= NP_001020.2:n.-249G=
NM_001029.5:c.-249G= MANE Select NP_001020.2:n.-249G=
XR_944989.3:n.86C=
XR_944990.3:n.86C=
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