Canonical Allele Identifier: CA363388740

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31914272C>A (hg19) ; chr6:g.31946495C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946495C>A , CM000668.2:g.31946495C>A	GRCh38
NC_000006.11:g.31914272C>A , CM000668.1:g.31914272C>A	GRCh37
NC_000006.10:g.32022251C>A	NCBI36
NG_008191.1:g.5552C>A , LRG_136:g.5552C>A
NG_011730.1:g.24007C>A , LRG_26:g.24007C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.364C>A
ENST00000483004.2:c.187C>A	ENSP00000419887.2:p.Pro63Thr
ENST00000497841.6:c.187C>A	ENSP00000513847.1:p.Pro63Thr
ENST00000698628.1:c.187C>A	ENSP00000513848.1:p.Pro63Thr
ENST00000698629.1:n.364C>A
ENST00000698630.1:n.348C>A
ENST00000698631.1:n.343C>A
ENST00000698632.1:n.315C>A
ENST00000698633.1:n.285C>A
ENST00000698636.1:n.409C>A
ENST00000425368.7:c.187C>A MANE Select	ENSP00000416561.2:p.Pro63Thr
ENST00000425368.6:c.187C>A	ENSP00000416561.2:p.Pro63Thr
ENST00000452035.6:n.187C>A
ENST00000456570.5:c.1693C>A	ENSP00000410815.1:p.Pro565Thr
ENST00000460718.5:c.74C>A	ENSP00000417793.1:p.Ser25Tyr
ENST00000472581.1:n.434C>A
ENST00000475617.5:c.187C>A	ENSP00000420090.1:p.Pro63Thr
ENST00000477310.1:c.1352-512C>A	ENSP00000418996.1:n.1352-512C>A
NM_001710.5:c.187C>A , LRG_136t1:c.187C>A	NP_001701.2:p.Pro63Thr
NM_001710.6:c.187C>A MANE Select	NP_001701.2:p.Pro63Thr