Canonical Allele Identifier: CA2038228931
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041602C= , CM000674.2:g.56041602C= GRCh38
NC_000012.11:g.56435386C= , CM000674.1:g.56435386C= GRCh37
NC_000012.10:g.54721653C= NCBI36
NG_023201.1:g.4701C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+206C= ENSP00000348849.5:n.-357+206C=
XR_944989.1:n.111G=
XR_944990.1:n.111G=
XR_944989.3:n.402G=
XR_944990.3:n.402G=