Canonical Allele Identifier: CA2122037946
Gene: OSGEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454820A= , CM000676.2:g.20454820A= GRCh38
NC_000014.8:g.20922979A= , CM000676.1:g.20922979A= GRCh37
NC_000014.7:g.19992819A= NCBI36
NG_008718.1:g.4690A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-137T= ENSP00000206542.4:n.-137T=
ENST00000556252.1:n.234T=
ENST00000556439.1:n.270T=
NM_017807.3:c.-137T= NP_060277.1:n.-137T=
XM_011536930.1:c.-198T= XP_011535232.1:n.-198T=
XM_011536931.1:c.-433T= XP_011535233.1:n.-433T=