Canonical Allele Identifier: CA2038228886
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041548T= , CM000674.2:g.56041548T= GRCh38
NC_000012.11:g.56435332T= , CM000674.1:g.56435332T= GRCh37
NC_000012.10:g.54721599T= NCBI36
NG_023201.1:g.4647T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+152T= ENSP00000348849.5:n.-357+152T=
XR_944989.1:n.165A=
XR_944990.1:n.165A=
XR_944989.3:n.456A=
XR_944990.3:n.456A=