Canonical Allele Identifier: CA2236942934
Gene: BCO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81280793A= , CM000678.2:g.81280793A= GRCh38
NC_000016.9:g.81314398A= , CM000678.1:g.81314398A= GRCh37
NC_000016.8:g.79871899A= NCBI36
NG_012171.1:g.47103A=

Transcript Alleles

HGVS Amino-acid change
ENST00000258168.7:c.1102-64A= MANE Select ENSP00000258168.2:n.1102-64A=
ENST00000258168.6:c.1102-64A= ENSP00000258168.2:n.1102-64A=
ENST00000563804.5:c.*726-64A= ENSP00000457910.1:n.*726-64A=
NM_017429.2:c.1102-64A= NP_059125.2:n.1102-64A=
XM_011523109.1:c.1102-6502A= XP_011521411.1:n.1102-6502A=
XM_011523110.1:c.553-64A= XP_011521412.1:n.553-64A=
XM_011523109.2:c.1102-6502A= XP_011521411.1:n.1102-6502A=
XM_017023286.2:c.1102-64A= XP_016878775.1:n.1102-64A=
XM_017023287.2:c.1102-64A= XP_016878776.1:n.1102-64A=
XM_017023288.2:c.1102-64A= XP_016878777.1:n.1102-64A=
XM_017023289.1:c.325-64A= XP_016878778.1:n.325-64A=
XR_002957813.1:n.1429-64A=
NM_017429.3:c.1102-64A= MANE Select NP_059125.2:n.1102-64A=