Canonical Allele Identifier: CA1148403740
Gene: RPS27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990759G= , CM000663.2:g.153990759G= GRCh38
NC_000001.10:g.153963235G= , CM000663.1:g.153963235G= GRCh37
NC_000001.9:g.152229859G= NCBI36
NG_053102.2:g.5005G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368567.4:c.-38G= ENSP00000357555.4:n.-38G=
NM_001349946.1:c.-255G= NP_001336875.1:n.-255G=
NM_001349947.1:c.-366G= NP_001336876.1:n.-366G=