Canonical Allele Identifier: CA363409747

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918665C>A (hg19) ; chr6:g.31950888C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950888C>A , CM000668.2:g.31950888C>A	GRCh38
NC_000006.11:g.31918665C>A , CM000668.1:g.31918665C>A	GRCh37
NC_000006.10:g.32026644C>A	NCBI36
NG_008191.1:g.9945C>A , LRG_136:g.9945C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2286C>A
ENST00000483004.2:c.1583C>A	ENSP00000419887.2:p.Thr528Asn
ENST00000698628.1:c.1625-256C>A	ENSP00000513848.1:n.1625-256C>A
ENST00000698629.1:n.2071C>A
ENST00000698630.1:n.2515C>A
ENST00000698631.1:n.2516C>A
ENST00000698632.1:n.3405C>A
ENST00000698633.1:n.3295C>A
ENST00000425368.7:c.1799C>A MANE Select	ENSP00000416561.2:p.Thr600Asn
ENST00000425368.6:c.1799C>A	ENSP00000416561.2:p.Thr600Asn
ENST00000456570.5:c.3305C>A	ENSP00000410815.1:p.Thr1102Asn
ENST00000467360.1:n.925C>A
ENST00000477310.1:c.2852C>A	ENSP00000418996.1:p.Thr951Asn
ENST00000482312.1:n.15C>A
ENST00000483004.1:c.421C>A
NM_001710.5:c.1799C>A , LRG_136t1:c.1799C>A	NP_001701.2:p.Thr600Asn
NM_001710.6:c.1799C>A MANE Select	NP_001701.2:p.Thr600Asn