Canonical Allele Identifier: CA2038228850
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041508T= , CM000674.2:g.56041508T= GRCh38
NC_000012.11:g.56435292T= , CM000674.1:g.56435292T= GRCh37
NC_000012.10:g.54721559T= NCBI36
NG_023201.1:g.4607T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+112T= ENSP00000348849.5:n.-357+112T=
XR_944989.1:n.205A=
XR_944990.1:n.205A=
XR_944989.3:n.496A=
XR_944990.3:n.496A=