Canonical Allele Identifier: CA2236942881

Gene: BCO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81280701G= , CM000678.2:g.81280701G=	GRCh38
NC_000016.9:g.81314306G= , CM000678.1:g.81314306G=	GRCh37
NC_000016.8:g.79871807G=	NCBI36
NG_012171.1:g.47011G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258168.7:c.1102-156G= MANE Select	ENSP00000258168.2:n.1102-156G=
ENST00000258168.6:c.1102-156G=	ENSP00000258168.2:n.1102-156G=
ENST00000563804.5:c.*726-156G=	ENSP00000457910.1:n.*726-156G=
NM_017429.2:c.1102-156G=	NP_059125.2:n.1102-156G=
XM_011523109.1:c.1102-6594G=	XP_011521411.1:n.1102-6594G=
XM_011523110.1:c.553-156G=	XP_011521412.1:n.553-156G=
XM_011523109.2:c.1102-6594G=	XP_011521411.1:n.1102-6594G=
XM_017023286.2:c.1102-156G=	XP_016878775.1:n.1102-156G=
XM_017023287.2:c.1102-156G=	XP_016878776.1:n.1102-156G=
XM_017023288.2:c.1102-156G=	XP_016878777.1:n.1102-156G=
XM_017023289.1:c.325-156G=	XP_016878778.1:n.325-156G=
XR_002957813.1:n.1429-156G=
NM_017429.3:c.1102-156G= MANE Select	NP_059125.2:n.1102-156G=