Canonical Allele Identifier: CA2236942938
Gene: BCO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81280812G= , CM000678.2:g.81280812G= GRCh38
NC_000016.9:g.81314417G= , CM000678.1:g.81314417G= GRCh37
NC_000016.8:g.79871918G= NCBI36
NG_012171.1:g.47122G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258168.7:c.1102-45G= MANE Select ENSP00000258168.2:n.1102-45G=
ENST00000258168.6:c.1102-45G= ENSP00000258168.2:n.1102-45G=
ENST00000563804.5:c.*726-45G= ENSP00000457910.1:n.*726-45G=
NM_017429.2:c.1102-45G= NP_059125.2:n.1102-45G=
XM_011523109.1:c.1102-6483G= XP_011521411.1:n.1102-6483G=
XM_011523110.1:c.553-45G= XP_011521412.1:n.553-45G=
XM_011523109.2:c.1102-6483G= XP_011521411.1:n.1102-6483G=
XM_017023286.2:c.1102-45G= XP_016878775.1:n.1102-45G=
XM_017023287.2:c.1102-45G= XP_016878776.1:n.1102-45G=
XM_017023288.2:c.1102-45G= XP_016878777.1:n.1102-45G=
XM_017023289.1:c.325-45G= XP_016878778.1:n.325-45G=
XR_002957813.1:n.1429-45G=
NM_017429.3:c.1102-45G= MANE Select NP_059125.2:n.1102-45G=