Canonical Allele Identifier: CA2038229165
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041784T= , CM000674.2:g.56041784T= GRCh38
NC_000012.11:g.56435568T= , CM000674.1:g.56435568T= GRCh37
NC_000012.10:g.54721835T= NCBI36
NG_023201.1:g.4883T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-27T= ENSP00000348849.5:n.-356-27T=
XR_944989.3:n.220A=
XR_944990.3:n.220A=