Canonical Allele Identifier: CA2122038011
Gene: OSGEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454896G= , CM000676.2:g.20454896G= GRCh38
NC_000014.8:g.20923055G= , CM000676.1:g.20923055G= GRCh37
NC_000014.7:g.19992895G= NCBI36
NG_008718.1:g.4766G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-213C= ENSP00000206542.4:n.-213C=
ENST00000556252.1:n.158C=
ENST00000556439.1:n.194C=
NM_017807.3:c.-213C= NP_060277.1:n.-213C=
XM_011536930.1:c.-274C= XP_011535232.1:n.-274C=