Canonical Allele Identifier: CA3728416

Gene: CFB

Linked Data

• dbSNP Id: rs751798144
• ExAC: 6:31918379 C / A
• gnomAD v2: 6-31918379-C-A
• gnomAD v4: 6-31950602-C-A
• MyVariant Identifiers: chr6:g.31918379C>A (hg19) ; chr6:g.31950602C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950602C>A , CM000668.2:g.31950602C>A	GRCh38
NC_000006.11:g.31918379C>A , CM000668.1:g.31918379C>A	GRCh37
NC_000006.10:g.32026358C>A	NCBI36
NG_008191.1:g.9659C>A , LRG_136:g.9659C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000452035.7:n.2000C>A
ENST00000483004.2:c.1409-17C>A	ENSP00000419887.2:n.1409-17C>A
ENST00000698628.1:c.1624+199C>A	ENSP00000513848.1:n.1624+199C>A
ENST00000698629.1:n.1802-17C>A
ENST00000698630.1:n.2341-17C>A
ENST00000698631.1:n.2342-17C>A
ENST00000698632.1:n.3119C>A
ENST00000698633.1:n.3009C>A
ENST00000698636.1:n.1847-17C>A
ENST00000425368.7:c.1625-17C>A MANE Select	ENSP00000416561.2:n.1625-17C>A
ENST00000425368.6:c.1625-17C>A	ENSP00000416561.2:n.1625-17C>A
ENST00000452035.6:n.1823C>A
ENST00000456570.5:c.3131-17C>A	ENSP00000410815.1:n.3131-17C>A
ENST00000467360.1:n.734C>A
ENST00000477310.1:c.2678-17C>A	ENSP00000418996.1:n.2678-17C>A
ENST00000483004.1:c.247-17C>A
NM_001710.5:c.1625-17C>A , LRG_136t1:c.1625-17C>A	NP_001701.2:n.1625-17C>A
NM_001710.6:c.1625-17C>A MANE Select	NP_001701.2:n.1625-17C>A