Canonical Allele Identifier: CA2122037876

Gene: OSGEP

Linked Data

• dbSNP Id: rs1594411049

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20454793G>C , CM000676.2:g.20454793G>C	GRCh38
NC_000014.8:g.20922952G>C , CM000676.1:g.20922952G>C	GRCh37
NC_000014.7:g.19992792G>C	NCBI36
NG_008718.1:g.4663G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206542.9:c.-110C>G MANE Select	ENSP00000206542.4:n.-110C>G
ENST00000206542.8:c.-110C>G	ENSP00000206542.4:n.-110C>G
ENST00000553640.3:c.-110C>G	ENSP00000451580.1:n.-110C>G
ENST00000554699.1:n.1C>G
ENST00000556252.1:n.261C>G
ENST00000556439.1:n.297C>G
NM_017807.3:c.-110C>G	NP_060277.1:n.-110C>G
XM_011536930.1:c.-171C>G	XP_011535232.1:n.-171C>G
XM_011536931.1:c.-406C>G	XP_011535233.1:n.-406C>G
XM_011536932.1:c.-410C>G	XP_011535234.1:n.-410C>G
NM_017807.4:c.-110C>G MANE Select	NP_060277.1:n.-110C>G