Canonical Allele Identifier: CA2122038017
Gene: OSGEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454899C= , CM000676.2:g.20454899C= GRCh38
NC_000014.8:g.20923058C= , CM000676.1:g.20923058C= GRCh37
NC_000014.7:g.19992898C= NCBI36
NG_008718.1:g.4769C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-216G= ENSP00000206542.4:n.-216G=
ENST00000556252.1:n.155G=
ENST00000556439.1:n.191G=
NM_017807.3:c.-216G= NP_060277.1:n.-216G=
XM_011536930.1:c.-277G= XP_011535232.1:n.-277G=