Canonical Allele Identifier: CA449811699

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31914202G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946425G>T , CM000668.2:g.31946425G>T	GRCh38
NC_000006.11:g.31914202G>T , CM000668.1:g.31914202G>T	GRCh37
NC_000006.10:g.32022181G>T	NCBI36
NG_008191.1:g.5482G>T , LRG_136:g.5482G>T
NG_011730.1:g.23937G>T , LRG_26:g.23937G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.294G>T
ENST00000483004.2:c.117G>T	ENSP00000419887.2:p.Leu39=
ENST00000497841.6:c.117G>T	ENSP00000513847.1:p.Leu39=
ENST00000698628.1:c.117G>T	ENSP00000513848.1:p.Leu39=
ENST00000698629.1:n.294G>T
ENST00000698630.1:n.278G>T
ENST00000698631.1:n.273G>T
ENST00000698632.1:n.245G>T
ENST00000698633.1:n.215G>T
ENST00000698636.1:n.339G>T
ENST00000425368.7:c.117G>T MANE Select	ENSP00000416561.2:p.Leu39=
ENST00000425368.6:c.117G>T	ENSP00000416561.2:p.Leu39=
ENST00000452035.6:n.117G>T
ENST00000456570.5:c.1623G>T	ENSP00000410815.1:p.Leu541=
ENST00000460718.5:c.65-61G>T	ENSP00000417793.1:n.65-61G>T
ENST00000472581.1:n.364G>T
ENST00000475617.5:c.117G>T	ENSP00000420090.1:p.Leu39=
ENST00000477310.1:c.1352-582G>T	ENSP00000418996.1:n.1352-582G>T
NM_001710.5:c.117G>T , LRG_136t1:c.117G>T	NP_001701.2:p.Leu39=
NM_001710.6:c.117G>T MANE Select	NP_001701.2:p.Leu39=