Canonical Allele Identifier: CA396872224

Gene: BCO1

Linked Data

• MyVariant Identifiers: chr16:g.81301601C>A (hg19) ; chr16:g.81267996C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81267996C>A , CM000678.2:g.81267996C>A	GRCh38
NC_000016.9:g.81301601C>A , CM000678.1:g.81301601C>A	GRCh37
NC_000016.8:g.79859102C>A	NCBI36
NG_012171.1:g.34306C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258168.7:c.708C>A MANE Select	ENSP00000258168.2:p.Tyr236Ter
ENST00000258168.6:c.708C>A	ENSP00000258168.2:p.Tyr236Ter
ENST00000563804.5:c.*332C>A	ENSP00000457910.1:n.*332C>A
NM_017429.2:c.708C>A	NP_059125.2:p.Tyr236Ter
XM_011523109.1:c.708C>A	XP_011521411.1:p.Tyr236Ter
XM_011523110.1:c.159C>A	XP_011521412.1:p.Tyr53Ter
XM_011523109.2:c.708C>A	XP_011521411.1:p.Tyr236Ter
XM_017023286.2:c.708C>A	XP_016878775.1:p.Tyr236Ter
XM_017023287.2:c.708C>A	XP_016878776.1:p.Tyr236Ter
XM_017023288.2:c.708C>A	XP_016878777.1:p.Tyr236Ter
XM_017023289.1:c.-24-46C>A	XP_016878778.1:n.-24-46C>A
XR_002957813.1:n.1081-46C>A
NM_017429.3:c.708C>A MANE Select	NP_059125.2:p.Tyr236Ter