Canonical Allele Identifier: CA363409227

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918516T>A (hg19) ; chr6:g.31950739T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950739T>A , CM000668.2:g.31950739T>A	GRCh38
NC_000006.11:g.31918516T>A , CM000668.1:g.31918516T>A	GRCh37
NC_000006.10:g.32026495T>A	NCBI36
NG_008191.1:g.9796T>A , LRG_136:g.9796T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2137T>A
ENST00000483004.2:c.1529T>A	ENSP00000419887.2:p.Leu510His
ENST00000698628.1:c.1624+336T>A	ENSP00000513848.1:n.1624+336T>A
ENST00000698629.1:n.1922T>A
ENST00000698630.1:n.2461T>A
ENST00000698631.1:n.2462T>A
ENST00000698632.1:n.3256T>A
ENST00000698633.1:n.3146T>A
ENST00000698636.1:n.1967T>A
ENST00000425368.7:c.1745T>A MANE Select	ENSP00000416561.2:p.Leu582His
ENST00000425368.6:c.1745T>A	ENSP00000416561.2:p.Leu582His
ENST00000456570.5:c.3251T>A	ENSP00000410815.1:p.Leu1084His
ENST00000467360.1:n.871T>A
ENST00000477310.1:c.2798T>A	ENSP00000418996.1:p.Leu933His
ENST00000483004.1:c.367T>A
NM_001710.5:c.1745T>A , LRG_136t1:c.1745T>A	NP_001701.2:p.Leu582His
NM_001710.6:c.1745T>A MANE Select	NP_001701.2:p.Leu582His