Canonical Allele Identifier: CA2038228894
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895879849
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041555A>T , CM000674.2:g.56041555A>T GRCh38
NC_000012.11:g.56435339A>T , CM000674.1:g.56435339A>T GRCh37
NC_000012.10:g.54721606A>T NCBI36
NG_023201.1:g.4654A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+159A>T ENSP00000348849.5:n.-357+159A>T
XR_944989.1:n.158T>A
XR_944990.1:n.158T>A
XR_944989.3:n.449T>A
XR_944990.3:n.449T>A
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