Canonical Allele Identifier: CA3728398

Gene: CFB

Linked Data

• dbSNP Id: rs770924117
• ExAC: 6:31918298 A / C
• gnomAD v2: 6-31918298-A-C
• gnomAD v3: 6-31950521-A-C
• gnomAD v4: 6-31950521-A-C
• MyVariant Identifiers: chr6:g.31918298A>C (hg19) ; chr6:g.31950521A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950521A>C , CM000668.2:g.31950521A>C	GRCh38
NC_000006.11:g.31918298A>C , CM000668.1:g.31918298A>C	GRCh37
NC_000006.10:g.32026277A>C	NCBI36
NG_008191.1:g.9578A>C , LRG_136:g.9578A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.1919A>C
ENST00000483004.2:c.1409-98A>C	ENSP00000419887.2:n.1409-98A>C
ENST00000698628.1:c.1624+118A>C	ENSP00000513848.1:n.1624+118A>C
ENST00000698629.1:n.1802-98A>C
ENST00000698630.1:n.2341-98A>C
ENST00000698631.1:n.2342-98A>C
ENST00000698632.1:n.3038A>C
ENST00000698633.1:n.2928A>C
ENST00000698636.1:n.1847-98A>C
ENST00000425368.7:c.1625-98A>C MANE Select	ENSP00000416561.2:n.1625-98A>C
ENST00000425368.6:c.1625-98A>C	ENSP00000416561.2:n.1625-98A>C
ENST00000452035.6:n.1742A>C
ENST00000456570.5:c.3131-98A>C	ENSP00000410815.1:n.3131-98A>C
ENST00000467360.1:n.653A>C
ENST00000477310.1:c.2678-98A>C	ENSP00000418996.1:n.2678-98A>C
ENST00000483004.1:c.247-98A>C
NM_001710.5:c.1625-98A>C , LRG_136t1:c.1625-98A>C	NP_001701.2:n.1625-98A>C
NM_001710.6:c.1625-98A>C MANE Select	NP_001701.2:n.1625-98A>C