Canonical Allele Identifier: CA2236989455
Gene: BCO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81267912C= , CM000678.2:g.81267912C= GRCh38
NC_000016.9:g.81301517C= , CM000678.1:g.81301517C= GRCh37
NC_000016.8:g.79859018C= NCBI36
NG_012171.1:g.34222C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258168.7:c.624C= MANE Select ENSP00000258168.2:p.Gly208=
ENST00000258168.6:c.624C= ENSP00000258168.2:p.Gly208=
ENST00000563804.5:c.*248C= ENSP00000457910.1:n.*248C=
NM_017429.2:c.624C= NP_059125.2:p.Gly208=
XM_011523109.1:c.624C= XP_011521411.1:p.Gly208=
XM_011523110.1:c.75C= XP_011521412.1:p.Gly25=
XM_011523109.2:c.624C= XP_011521411.1:p.Gly208=
XM_017023286.2:c.624C= XP_016878775.1:p.Gly208=
XM_017023287.2:c.624C= XP_016878776.1:p.Gly208=
XM_017023288.2:c.624C= XP_016878777.1:p.Gly208=
XM_017023289.1:c.-24-130C= XP_016878778.1:n.-24-130C=
XR_002957813.1:n.1081-130C=
NM_017429.3:c.624C= MANE Select NP_059125.2:p.Gly208=