Canonical Allele Identifier: CA396876711

Gene: BCO1

Linked Data

• dbSNP Id: rs1335989638
• MyVariant Identifiers: chr16:g.81314460A>C (hg19) ; chr16:g.81280855A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81280855A>C , CM000678.2:g.81280855A>C	GRCh38
NC_000016.9:g.81314460A>C , CM000678.1:g.81314460A>C	GRCh37
NC_000016.8:g.79871961A>C	NCBI36
NG_012171.1:g.47165A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258168.7:c.1102-2A>C MANE Select	ENSP00000258168.2:n.1102-2A>C
ENST00000258168.6:c.1102-2A>C	ENSP00000258168.2:n.1102-2A>C
ENST00000563804.5:c.*726-2A>C	ENSP00000457910.1:n.*726-2A>C
NM_017429.2:c.1102-2A>C	NP_059125.2:n.1102-2A>C
XM_011523109.1:c.1102-6440A>C	XP_011521411.1:n.1102-6440A>C
XM_011523110.1:c.553-2A>C	XP_011521412.1:n.553-2A>C
XM_011523109.2:c.1102-6440A>C	XP_011521411.1:n.1102-6440A>C
XM_017023286.2:c.1102-2A>C	XP_016878775.1:n.1102-2A>C
XM_017023287.2:c.1102-2A>C	XP_016878776.1:n.1102-2A>C
XM_017023288.2:c.1102-2A>C	XP_016878777.1:n.1102-2A>C
XM_017023289.1:c.325-2A>C	XP_016878778.1:n.325-2A>C
XR_002957813.1:n.1429-2A>C
NM_017429.3:c.1102-2A>C MANE Select	NP_059125.2:n.1102-2A>C