Canonical Allele Identifier: CA136898158

Gene: CFB

Linked Data

• dbSNP Id: rs878962361
• MyVariant Identifiers: chr6:g.31918916T>A (hg19) ; chr6:g.31951139T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951139T>A , CM000668.2:g.31951139T>A	GRCh38
NC_000006.11:g.31918916T>A , CM000668.1:g.31918916T>A	GRCh37
NC_000006.10:g.32026895T>A	NCBI36
NG_008191.1:g.10196T>A , LRG_136:g.10196T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-58T>A
ENST00000483004.2:c.1640-5T>A	ENSP00000419887.2:n.1640-5T>A
ENST00000698628.1:c.1625-5T>A	ENSP00000513848.1:n.1625-5T>A
ENST00000698629.1:n.2128-58T>A
ENST00000698630.1:n.2572-5T>A
ENST00000698631.1:n.2573-5T>A
ENST00000698632.1:n.3656T>A
ENST00000698633.1:n.3546T>A
ENST00000425368.7:c.1856-5T>A MANE Select	ENSP00000416561.2:n.1856-5T>A
ENST00000425368.6:c.1856-5T>A	ENSP00000416561.2:n.1856-5T>A
ENST00000456570.5:c.3362-5T>A	ENSP00000410815.1:n.3362-5T>A
ENST00000467360.1:n.982-5T>A
ENST00000477310.1:c.2909-5T>A	ENSP00000418996.1:n.2909-5T>A
ENST00000482312.1:n.266T>A
ENST00000483004.1:c.478-5T>A
NM_001710.5:c.1856-5T>A , LRG_136t1:c.1856-5T>A	NP_001701.2:n.1856-5T>A
NM_001710.6:c.1856-5T>A MANE Select	NP_001701.2:n.1856-5T>A