Canonical Allele Identifier: CA363389605

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31914350G>A (hg19) ; chr6:g.31946573G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946573G>A , CM000668.2:g.31946573G>A	GRCh38
NC_000006.11:g.31914350G>A , CM000668.1:g.31914350G>A	GRCh37
NC_000006.10:g.32022329G>A	NCBI36
NG_008191.1:g.5630G>A , LRG_136:g.5630G>A
NG_011730.1:g.24085G>A , LRG_26:g.24085G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.442G>A
ENST00000483004.2:c.265G>A	ENSP00000419887.2:p.Asp89Asn
ENST00000497841.6:c.265G>A	ENSP00000513847.1:p.Asp89Asn
ENST00000698628.1:c.265G>A	ENSP00000513848.1:p.Asp89Asn
ENST00000698629.1:n.442G>A
ENST00000698630.1:n.426G>A
ENST00000698631.1:n.421G>A
ENST00000698632.1:n.393G>A
ENST00000698633.1:n.363G>A
ENST00000698636.1:n.487G>A
ENST00000425368.7:c.265G>A MANE Select	ENSP00000416561.2:p.Asp89Asn
ENST00000425368.6:c.265G>A	ENSP00000416561.2:p.Asp89Asn
ENST00000452035.6:n.265G>A
ENST00000456570.5:c.1771G>A	ENSP00000410815.1:p.Asp591Asn
ENST00000460718.5:c.152G>A	ENSP00000417793.1:p.Arg51Lys
ENST00000472581.1:n.512G>A
ENST00000475617.5:c.265G>A	ENSP00000420090.1:p.Asp89Asn
ENST00000477310.1:c.1352-434G>A	ENSP00000418996.1:n.1352-434G>A
NM_001710.5:c.265G>A , LRG_136t1:c.265G>A	NP_001701.2:p.Asp89Asn
NM_001710.6:c.265G>A MANE Select	NP_001701.2:p.Asp89Asn