Canonical Allele Identifier: CA2581159026
Gene: OSGEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454848C>G , CM000676.2:g.20454848C>G GRCh38
NC_000014.8:g.20923007C>G , CM000676.1:g.20923007C>G GRCh37
NC_000014.7:g.19992847C>G NCBI36
NG_008718.1:g.4718C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-165G>C ENSP00000206542.4:n.-165G>C
ENST00000556252.1:n.206G>C
ENST00000556439.1:n.242G>C
NM_017807.3:c.-165G>C NP_060277.1:n.-165G>C
XM_011536930.1:c.-226G>C XP_011535232.1:n.-226G>C