Canonical Allele Identifier: CA3728481

Gene: CFB

Linked Data

• ClinVar Variation Id: 1167164
• ClinVar RCV Id: RCV001516137
• dbSNP Id: rs4151671
• ExAC: 6:31918903 C / T
• gnomAD v2: 6-31918903-C-T
• gnomAD v3: 6-31951126-C-T
• gnomAD v4: 6-31951126-C-T
• MyVariant Identifiers: chr6:g.31918903C>T (hg19) ; chr6:g.31951126C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951126C>T , CM000668.2:g.31951126C>T	GRCh38
NC_000006.11:g.31918903C>T , CM000668.1:g.31918903C>T	GRCh37
NC_000006.10:g.32026882C>T	NCBI36
NG_008191.1:g.10183C>T , LRG_136:g.10183C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-71C>T
ENST00000483004.2:c.1640-18C>T	ENSP00000419887.2:n.1640-18C>T
ENST00000698628.1:c.1625-18C>T	ENSP00000513848.1:n.1625-18C>T
ENST00000698629.1:n.2128-71C>T
ENST00000698630.1:n.2572-18C>T
ENST00000698631.1:n.2573-18C>T
ENST00000698632.1:n.3643C>T
ENST00000698633.1:n.3533C>T
ENST00000425368.7:c.1856-18C>T MANE Select	ENSP00000416561.2:n.1856-18C>T
ENST00000425368.6:c.1856-18C>T	ENSP00000416561.2:n.1856-18C>T
ENST00000456570.5:c.3362-18C>T	ENSP00000410815.1:n.3362-18C>T
ENST00000467360.1:n.982-18C>T
ENST00000477310.1:c.2909-18C>T	ENSP00000418996.1:n.2909-18C>T
ENST00000482312.1:n.253C>T
ENST00000483004.1:c.478-18C>T
NM_001710.5:c.1856-18C>T , LRG_136t1:c.1856-18C>T	NP_001701.2:n.1856-18C>T
NM_001710.6:c.1856-18C>T MANE Select	NP_001701.2:n.1856-18C>T