Canonical Allele Identifier: CA2122037996
Gene: OSGEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454878C= , CM000676.2:g.20454878C= GRCh38
NC_000014.8:g.20923037C= , CM000676.1:g.20923037C= GRCh37
NC_000014.7:g.19992877C= NCBI36
NG_008718.1:g.4748C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-195G= ENSP00000206542.4:n.-195G=
ENST00000556252.1:n.176G=
ENST00000556439.1:n.212G=
NM_017807.3:c.-195G= NP_060277.1:n.-195G=
XM_011536930.1:c.-256G= XP_011535232.1:n.-256G=