Canonical Allele Identifier: CA2038228895
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041557A= , CM000674.2:g.56041557A= GRCh38
NC_000012.11:g.56435341A= , CM000674.1:g.56435341A= GRCh37
NC_000012.10:g.54721608A= NCBI36
NG_023201.1:g.4656A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+161A= ENSP00000348849.5:n.-357+161A=
XR_944989.1:n.156T=
XR_944990.1:n.156T=
XR_944989.3:n.447T=
XR_944990.3:n.447T=