Canonical Allele Identifier: CA2480680206
Gene: RPS27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990761T= , CM000663.2:g.153990761T= GRCh38
NC_000001.10:g.153963237T= , CM000663.1:g.153963237T= GRCh37
NC_000001.9:g.152229861T= NCBI36
NG_053102.2:g.5007T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368567.4:c.-36T= ENSP00000357555.4:n.-36T=
NM_001349946.1:c.-253T= NP_001336875.1:n.-253T=
NM_001349947.1:c.-364T= NP_001336876.1:n.-364T=