Canonical Allele Identifier: CA2122038032
Gene: OSGEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454908T= , CM000676.2:g.20454908T= GRCh38
NC_000014.8:g.20923067T= , CM000676.1:g.20923067T= GRCh37
NC_000014.7:g.19992907T= NCBI36
NG_008718.1:g.4778T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-225A= ENSP00000206542.4:n.-225A=
ENST00000556252.1:n.146A=
ENST00000556439.1:n.182A=
NM_017807.3:c.-225A= NP_060277.1:n.-225A=
XM_011536930.1:c.-286A= XP_011535232.1:n.-286A=