Canonical Allele Identifier: CA449811669

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31914166A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946389A>T , CM000668.2:g.31946389A>T	GRCh38
NC_000006.11:g.31914166A>T , CM000668.1:g.31914166A>T	GRCh37
NC_000006.10:g.32022145A>T	NCBI36
NG_008191.1:g.5446A>T , LRG_136:g.5446A>T
NG_011730.1:g.23901A>T , LRG_26:g.23901A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.258A>T
ENST00000483004.2:c.81A>T	ENSP00000419887.2:p.Pro27=
ENST00000497841.6:c.81A>T	ENSP00000513847.1:p.Pro27=
ENST00000698628.1:c.81A>T	ENSP00000513848.1:p.Pro27=
ENST00000698629.1:n.258A>T
ENST00000698630.1:n.242A>T
ENST00000698631.1:n.237A>T
ENST00000698632.1:n.209A>T
ENST00000698633.1:n.179A>T
ENST00000698636.1:n.303A>T
ENST00000425368.7:c.81A>T MANE Select	ENSP00000416561.2:p.Pro27=
ENST00000425368.6:c.81A>T	ENSP00000416561.2:p.Pro27=
ENST00000452035.6:n.81A>T
ENST00000456570.5:c.1587A>T	ENSP00000410815.1:p.Pro529=
ENST00000460718.5:c.65-97A>T	ENSP00000417793.1:n.65-97A>T
ENST00000472581.1:n.328A>T
ENST00000475617.5:c.81A>T	ENSP00000420090.1:p.Pro27=
ENST00000477310.1:c.1352-618A>T	ENSP00000418996.1:n.1352-618A>T
NM_001710.5:c.81A>T , LRG_136t1:c.81A>T	NP_001701.2:p.Pro27=
NM_001710.6:c.81A>T MANE Select	NP_001701.2:p.Pro27=