Canonical Allele Identifier: CA1142411338
Gene: RPS27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990760C= , CM000663.2:g.153990760C= GRCh38
NC_000001.10:g.153963236C= , CM000663.1:g.153963236C= GRCh37
NC_000001.9:g.152229860C= NCBI36
NG_053102.2:g.5006C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368567.4:c.-37C= ENSP00000357555.4:n.-37C=
NM_001349946.1:c.-254C= NP_001336875.1:n.-254C=
NM_001349947.1:c.-365C= NP_001336876.1:n.-365C=