Canonical Allele Identifier: CA1143586889
Gene: RPS27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990757T= , CM000663.2:g.153990757T= GRCh38
NC_000001.10:g.153963233T= , CM000663.1:g.153963233T= GRCh37
NC_000001.9:g.152229857T= NCBI36
NG_053102.2:g.5003T=

Transcript Alleles

HGVS Amino-acid Change
NM_001349946.1:c.-257T= NP_001336875.1:n.-257T=
NM_001349947.1:c.-368T= NP_001336876.1:n.-368T=