Canonical Allele Identifier: CA2624006049

Gene: OSGEP

Linked Data

• gnomAD v4: 14-20454833-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20454833C>A , CM000676.2:g.20454833C>A	GRCh38
NC_000014.8:g.20922992C>A , CM000676.1:g.20922992C>A	GRCh37
NC_000014.7:g.19992832C>A	NCBI36
NG_008718.1:g.4703C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206542.8:c.-150G>T	ENSP00000206542.4:n.-150G>T
ENST00000556252.1:n.221G>T
ENST00000556439.1:n.257G>T
NM_017807.3:c.-150G>T	NP_060277.1:n.-150G>T
XM_011536930.1:c.-211G>T	XP_011535232.1:n.-211G>T
XM_011536931.1:c.-446G>T	XP_011535233.1:n.-446G>T