Canonical Allele Identifier: CA363410210

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918713A>C (hg19) ; chr6:g.31950936A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950936A>C , CM000668.2:g.31950936A>C	GRCh38
NC_000006.11:g.31918713A>C , CM000668.1:g.31918713A>C	GRCh37
NC_000006.10:g.32026692A>C	NCBI36
NG_008191.1:g.9993A>C , LRG_136:g.9993A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2334A>C
ENST00000483004.2:c.1631A>C	ENSP00000419887.2:p.Gln544Pro
ENST00000698628.1:c.1625-208A>C	ENSP00000513848.1:n.1625-208A>C
ENST00000698629.1:n.2119A>C
ENST00000698630.1:n.2563A>C
ENST00000698631.1:n.2564A>C
ENST00000698632.1:n.3453A>C
ENST00000698633.1:n.3343A>C
ENST00000425368.7:c.1847A>C MANE Select	ENSP00000416561.2:p.Gln616Pro
ENST00000425368.6:c.1847A>C	ENSP00000416561.2:p.Gln616Pro
ENST00000456570.5:c.3353A>C	ENSP00000410815.1:p.Gln1118Pro
ENST00000467360.1:n.973A>C
ENST00000477310.1:c.2900A>C	ENSP00000418996.1:p.Gln967Pro
ENST00000482312.1:n.63A>C
ENST00000483004.1:c.469A>C
NM_001710.5:c.1847A>C , LRG_136t1:c.1847A>C	NP_001701.2:p.Gln616Pro
NM_001710.6:c.1847A>C MANE Select	NP_001701.2:p.Gln616Pro