Canonical Allele Identifier: CA412439624

Gene: FANCB

Linked Data

• MyVariant Identifiers: chrX:g.14863118G>C (hg19) ; chrX:g.14844996G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.14844996G>C , CM000685.2:g.14844996G>C	GRCh38
NC_000023.10:g.14863118G>C , CM000685.1:g.14863118G>C	GRCh37
NC_000023.9:g.14773039G>C	NCBI36
NG_007310.1:g.33067C>G , LRG_496:g.33067C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000452869.2:c.1787C>G	ENSP00000397849.2:p.Thr596Ser
ENST00000643728.2:c.*866C>G	ENSP00000495047.1:n.*866C>G
ENST00000696311.1:c.1787C>G	ENSP00000512549.1:p.Thr596Ser
ENST00000696312.1:c.1787C>G	ENSP00000512550.1:p.Thr596Ser
ENST00000696322.1:c.1160C>G
ENST00000696351.1:c.1787C>G	ENSP00000512572.1:p.Thr596Ser
ENST00000696352.1:c.1787C>G	ENSP00000512573.1:p.Thr596Ser
ENST00000696353.1:c.1787C>G	ENSP00000512574.1:p.Thr596Ser
ENST00000696354.1:c.1787C>G	ENSP00000512575.1:p.Thr596Ser
ENST00000696355.1:c.1497-256C>G	ENSP00000512576.1:n.1497-256C>G
ENST00000696356.1:c.1787C>G	ENSP00000512577.1:p.Thr596Ser
ENST00000696357.1:c.1787C>G	ENSP00000512578.1:p.Thr596Ser
ENST00000643728.1:c.*866C>G	ENSP00000495047.1:n.*866C>G
ENST00000646255.1:c.*779C>G	ENSP00000494963.1:n.*779C>G
ENST00000650831.1:c.1787C>G MANE Select	ENSP00000498215.1:p.Thr596Ser
ENST00000324138.7:c.1787C>G	ENSP00000326819.3:p.Thr596Ser
ENST00000398334.5:c.1787C>G	ENSP00000381378.1:p.Thr596Ser
ENST00000452869.1:c.1787C>G	ENSP00000397849.1:p.Thr596Ser
NM_001018113.1:c.1787C>G , LRG_496t1:c.1787C>G	NP_001018123.1:p.Thr596Ser
NM_152633.2:c.1787C>G	NP_689846.1:p.Thr596Ser
XM_011545470.1:c.1787C>G	XP_011543772.1:p.Thr596Ser
NM_001018113.2:c.1787C>G	NP_001018123.1:p.Thr596Ser
NM_001324162.1:c.1787C>G	NP_001311091.1:p.Thr596Ser
NM_152633.3:c.1787C>G	NP_689846.1:p.Thr596Ser
XM_011545470.2:c.1787C>G	XP_011543772.1:p.Thr596Ser
XM_017029355.2:c.1787C>G	XP_016884844.1:p.Thr596Ser
XM_017029356.1:c.1787C>G	XP_016884845.1:p.Thr596Ser
XR_001755672.1:n.2248C>G
XR_001755673.1:n.2040C>G
XR_001755674.1:n.1941C>G
NM_001018113.3:c.1787C>G MANE Select	NP_001018123.1:p.Thr596Ser
NM_001324162.2:c.1787C>G	NP_001311091.1:p.Thr596Ser
NM_152633.4:c.1787C>G	NP_689846.1:p.Thr596Ser