Canonical Allele Identifier: CA136898205

Gene: CFB

Linked Data

• dbSNP Id: rs113885316
• gnomAD v4: 6-31951143-G-A
• MyVariant Identifiers: chr6:g.31918920G>A (hg19) ; chr6:g.31951143G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951143G>A , CM000668.2:g.31951143G>A	GRCh38
NC_000006.11:g.31918920G>A , CM000668.1:g.31918920G>A	GRCh37
NC_000006.10:g.32026899G>A	NCBI36
NG_008191.1:g.10200G>A , LRG_136:g.10200G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-54G>A
ENST00000483004.2:c.1640-1G>A	ENSP00000419887.2:n.1640-1G>A
ENST00000698628.1:c.1625-1G>A	ENSP00000513848.1:n.1625-1G>A
ENST00000698629.1:n.2128-54G>A
ENST00000698630.1:n.2572-1G>A
ENST00000698631.1:n.2573-1G>A
ENST00000698632.1:n.3660G>A
ENST00000698633.1:n.3550G>A
ENST00000425368.7:c.1856-1G>A MANE Select	ENSP00000416561.2:n.1856-1G>A
ENST00000425368.6:c.1856-1G>A	ENSP00000416561.2:n.1856-1G>A
ENST00000456570.5:c.3362-1G>A	ENSP00000410815.1:n.3362-1G>A
ENST00000467360.1:n.982-1G>A
ENST00000477310.1:c.2909-1G>A	ENSP00000418996.1:n.2909-1G>A
ENST00000482312.1:n.270G>A
ENST00000483004.1:c.478-1G>A
NM_001710.5:c.1856-1G>A , LRG_136t1:c.1856-1G>A	NP_001701.2:n.1856-1G>A
NM_001710.6:c.1856-1G>A MANE Select	NP_001701.2:n.1856-1G>A