Canonical Allele Identifier: CA396871612

Gene: BCO1

Linked Data

• MyVariant Identifiers: chr16:g.81301549C>A (hg19) ; chr16:g.81267944C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81267944C>A , CM000678.2:g.81267944C>A	GRCh38
NC_000016.9:g.81301549C>A , CM000678.1:g.81301549C>A	GRCh37
NC_000016.8:g.79859050C>A	NCBI36
NG_012171.1:g.34254C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258168.7:c.656C>A MANE Select	ENSP00000258168.2:p.Thr219Lys
ENST00000258168.6:c.656C>A	ENSP00000258168.2:p.Thr219Lys
ENST00000563804.5:c.*280C>A	ENSP00000457910.1:n.*280C>A
NM_017429.2:c.656C>A	NP_059125.2:p.Thr219Lys
XM_011523109.1:c.656C>A	XP_011521411.1:p.Thr219Lys
XM_011523110.1:c.107C>A	XP_011521412.1:p.Thr36Lys
XM_011523109.2:c.656C>A	XP_011521411.1:p.Thr219Lys
XM_017023286.2:c.656C>A	XP_016878775.1:p.Thr219Lys
XM_017023287.2:c.656C>A	XP_016878776.1:p.Thr219Lys
XM_017023288.2:c.656C>A	XP_016878777.1:p.Thr219Lys
XM_017023289.1:c.-24-98C>A	XP_016878778.1:n.-24-98C>A
XR_002957813.1:n.1081-98C>A
NM_017429.3:c.656C>A MANE Select	NP_059125.2:p.Thr219Lys