Canonical Allele Identifier: CA363409733

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918662G>C (hg19) ; chr6:g.31950885G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950885G>C , CM000668.2:g.31950885G>C	GRCh38
NC_000006.11:g.31918662G>C , CM000668.1:g.31918662G>C	GRCh37
NC_000006.10:g.32026641G>C	NCBI36
NG_008191.1:g.9942G>C , LRG_136:g.9942G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2283G>C
ENST00000483004.2:c.1580G>C	ENSP00000419887.2:p.Cys527Ser
ENST00000698628.1:c.1625-259G>C	ENSP00000513848.1:n.1625-259G>C
ENST00000698629.1:n.2068G>C
ENST00000698630.1:n.2512G>C
ENST00000698631.1:n.2513G>C
ENST00000698632.1:n.3402G>C
ENST00000698633.1:n.3292G>C
ENST00000425368.7:c.1796G>C MANE Select	ENSP00000416561.2:p.Cys599Ser
ENST00000425368.6:c.1796G>C	ENSP00000416561.2:p.Cys599Ser
ENST00000456570.5:c.3302G>C	ENSP00000410815.1:p.Cys1101Ser
ENST00000467360.1:n.922G>C
ENST00000477310.1:c.2849G>C	ENSP00000418996.1:p.Cys950Ser
ENST00000482312.1:n.12G>C
ENST00000483004.1:c.418G>C
NM_001710.5:c.1796G>C , LRG_136t1:c.1796G>C	NP_001701.2:p.Cys599Ser
NM_001710.6:c.1796G>C MANE Select	NP_001701.2:p.Cys599Ser