Canonical Allele Identifier: CA363408839

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918448C>A (hg19) ; chr6:g.31950671C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950671C>A , CM000668.2:g.31950671C>A	GRCh38
NC_000006.11:g.31918448C>A , CM000668.1:g.31918448C>A	GRCh37
NC_000006.10:g.32026427C>A	NCBI36
NG_008191.1:g.9728C>A , LRG_136:g.9728C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2069C>A
ENST00000483004.2:c.1461C>A	ENSP00000419887.2:p.Tyr487Ter
ENST00000698628.1:c.1624+268C>A	ENSP00000513848.1:n.1624+268C>A
ENST00000698629.1:n.1854C>A
ENST00000698630.1:n.2393C>A
ENST00000698631.1:n.2394C>A
ENST00000698632.1:n.3188C>A
ENST00000698633.1:n.3078C>A
ENST00000698636.1:n.1899C>A
ENST00000425368.7:c.1677C>A MANE Select	ENSP00000416561.2:p.Tyr559Ter
ENST00000425368.6:c.1677C>A	ENSP00000416561.2:p.Tyr559Ter
ENST00000456570.5:c.3183C>A	ENSP00000410815.1:p.Tyr1061Ter
ENST00000467360.1:n.803C>A
ENST00000477310.1:c.2730C>A	ENSP00000418996.1:p.Tyr910Ter
ENST00000483004.1:c.299C>A
NM_001710.5:c.1677C>A , LRG_136t1:c.1677C>A	NP_001701.2:p.Tyr559Ter
NM_001710.6:c.1677C>A MANE Select	NP_001701.2:p.Tyr559Ter