Canonical Allele Identifier: CA363409820

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918674C>T (hg19) ; chr6:g.31950897C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950897C>T , CM000668.2:g.31950897C>T	GRCh38
NC_000006.11:g.31918674C>T , CM000668.1:g.31918674C>T	GRCh37
NC_000006.10:g.32026653C>T	NCBI36
NG_008191.1:g.9954C>T , LRG_136:g.9954C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2295C>T
ENST00000483004.2:c.1592C>T	ENSP00000419887.2:p.Thr531Ile
ENST00000698628.1:c.1625-247C>T	ENSP00000513848.1:n.1625-247C>T
ENST00000698629.1:n.2080C>T
ENST00000698630.1:n.2524C>T
ENST00000698631.1:n.2525C>T
ENST00000698632.1:n.3414C>T
ENST00000698633.1:n.3304C>T
ENST00000425368.7:c.1808C>T MANE Select	ENSP00000416561.2:p.Thr603Ile
ENST00000425368.6:c.1808C>T	ENSP00000416561.2:p.Thr603Ile
ENST00000456570.5:c.3314C>T	ENSP00000410815.1:p.Thr1105Ile
ENST00000467360.1:n.934C>T
ENST00000477310.1:c.2861C>T	ENSP00000418996.1:p.Thr954Ile
ENST00000482312.1:n.24C>T
ENST00000483004.1:c.430C>T
NM_001710.5:c.1808C>T , LRG_136t1:c.1808C>T	NP_001701.2:p.Thr603Ile
NM_001710.6:c.1808C>T MANE Select	NP_001701.2:p.Thr603Ile