Canonical Allele Identifier: CA2038229019
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041688G= , CM000674.2:g.56041688G= GRCh38
NC_000012.11:g.56435472G= , CM000674.1:g.56435472G= GRCh37
NC_000012.10:g.54721739G= NCBI36
NG_023201.1:g.4787G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-123G= ENSP00000348849.5:n.-356-123G=
XR_944989.1:n.25C=
XR_944990.1:n.25C=
XR_944989.3:n.316C=
XR_944990.3:n.316C=