Canonical Allele Identifier: CA2122038014
Gene: OSGEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454898G= , CM000676.2:g.20454898G= GRCh38
NC_000014.8:g.20923057G= , CM000676.1:g.20923057G= GRCh37
NC_000014.7:g.19992897G= NCBI36
NG_008718.1:g.4768G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-215C= ENSP00000206542.4:n.-215C=
ENST00000556252.1:n.156C=
ENST00000556439.1:n.192C=
NM_017807.3:c.-215C= NP_060277.1:n.-215C=
XM_011536930.1:c.-276C= XP_011535232.1:n.-276C=