Canonical Allele Identifier: CA2038229014
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041682G= , CM000674.2:g.56041682G= GRCh38
NC_000012.11:g.56435466G= , CM000674.1:g.56435466G= GRCh37
NC_000012.10:g.54721733G= NCBI36
NG_023201.1:g.4781G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-129G= ENSP00000348849.5:n.-356-129G=
XR_944989.1:n.31C=
XR_944990.1:n.31C=
XR_944989.3:n.322C=
XR_944990.3:n.322C=