Canonical Allele Identifier: CA363409003

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918477T>G (hg19) ; chr6:g.31950700T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950700T>G , CM000668.2:g.31950700T>G	GRCh38
NC_000006.11:g.31918477T>G , CM000668.1:g.31918477T>G	GRCh37
NC_000006.10:g.32026456T>G	NCBI36
NG_008191.1:g.9757T>G , LRG_136:g.9757T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000452035.7:n.2098T>G
ENST00000483004.2:c.1490T>G	ENSP00000419887.2:p.Ile497Ser
ENST00000698628.1:c.1624+297T>G	ENSP00000513848.1:n.1624+297T>G
ENST00000698629.1:n.1883T>G
ENST00000698630.1:n.2422T>G
ENST00000698631.1:n.2423T>G
ENST00000698632.1:n.3217T>G
ENST00000698633.1:n.3107T>G
ENST00000698636.1:n.1928T>G
ENST00000425368.7:c.1706T>G MANE Select	ENSP00000416561.2:p.Ile569Ser
ENST00000425368.6:c.1706T>G	ENSP00000416561.2:p.Ile569Ser
ENST00000456570.5:c.3212T>G	ENSP00000410815.1:p.Ile1071Ser
ENST00000467360.1:n.832T>G
ENST00000477310.1:c.2759T>G	ENSP00000418996.1:p.Ile920Ser
ENST00000483004.1:c.328T>G
NM_001710.5:c.1706T>G , LRG_136t1:c.1706T>G	NP_001701.2:p.Ile569Ser
NM_001710.6:c.1706T>G MANE Select	NP_001701.2:p.Ile569Ser