Canonical Allele Identifier: CA363409984

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918692T>C (hg19) ; chr6:g.31950915T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950915T>C , CM000668.2:g.31950915T>C	GRCh38
NC_000006.11:g.31918692T>C , CM000668.1:g.31918692T>C	GRCh37
NC_000006.10:g.32026671T>C	NCBI36
NG_008191.1:g.9972T>C , LRG_136:g.9972T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2313T>C
ENST00000483004.2:c.1610T>C	ENSP00000419887.2:p.Leu537Pro
ENST00000698628.1:c.1625-229T>C	ENSP00000513848.1:n.1625-229T>C
ENST00000698629.1:n.2098T>C
ENST00000698630.1:n.2542T>C
ENST00000698631.1:n.2543T>C
ENST00000698632.1:n.3432T>C
ENST00000698633.1:n.3322T>C
ENST00000425368.7:c.1826T>C MANE Select	ENSP00000416561.2:p.Leu609Pro
ENST00000425368.6:c.1826T>C	ENSP00000416561.2:p.Leu609Pro
ENST00000456570.5:c.3332T>C	ENSP00000410815.1:p.Leu1111Pro
ENST00000467360.1:n.952T>C
ENST00000477310.1:c.2879T>C	ENSP00000418996.1:p.Leu960Pro
ENST00000482312.1:n.42T>C
ENST00000483004.1:c.448T>C
NM_001710.5:c.1826T>C , LRG_136t1:c.1826T>C	NP_001701.2:p.Leu609Pro
NM_001710.6:c.1826T>C MANE Select	NP_001701.2:p.Leu609Pro