Canonical Allele Identifier: CA915950773

Gene: FANCB

Linked Data

• ClinVar Variation Id: 691306
• ClinVar RCV Id: RCV000851561

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.14843567_14845286del , CM000685.2:g.14843567_14845286del	GRCh38
NC_000023.10:g.14861689_14863408del , CM000685.1:g.14861689_14863408del	GRCh37
NC_000023.9:g.14771610_14773329del	NCBI36
NG_007310.1:g.32777_34496del , LRG_496:g.32777_34496del

Transcript Alleles

HGVS	Amino-acid change
ENST00000452869.2:c.1497_2487+93del
ENST00000643728.2:c.*576_*1566+93del
ENST00000696311.1:c.1497_2487+93del
ENST00000696312.1:c.1497_2580del
ENST00000696322.1:c.870_1860+93del
ENST00000696351.1:c.1497_2487+93del
ENST00000696352.1:c.1497_2487+93del
ENST00000696353.1:c.1497_2487+93del
ENST00000696354.1:c.1497_2487+93del
ENST00000696355.1:c.1497-546_*517+93del
ENST00000696356.1:c.1497_2580del
ENST00000696357.1:c.1497_2580del
ENST00000643728.1:c.*576_*1566+93del
ENST00000646255.1:c.*489_*1572del
ENST00000650831.1:c.1497_2580del
ENST00000324138.7:c.1497_2580del
ENST00000398334.5:c.1497_2580del
NM_001018113.1:c.1497_2580del , LRG_496t1:c.1497_2580del
NM_152633.2:c.1497_2580del
XM_011545470.1:c.1497_2487+93del
NM_001018113.2:c.1497_2580del
NM_001324162.1:c.1497_2580del
NM_152633.3:c.1497_2580del
XM_011545470.2:c.1497_2487+93del
XM_017029355.2:c.1497_2580del
XM_017029356.1:c.1497_2487+93del
XR_001755672.1:n.1958_2948+93del
XR_001755673.1:n.1750_2740+93del
XR_001755674.1:n.1651_2641+93del
NM_001018113.3:c.1497_2580del
NM_001324162.2:c.1497_2580del
NM_152633.4:c.1497_2580del