Canonical Allele Identifier: CA363408539

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918395G>T (hg19) ; chr6:g.31950618G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950618G>T , CM000668.2:g.31950618G>T	GRCh38
NC_000006.11:g.31918395G>T , CM000668.1:g.31918395G>T	GRCh37
NC_000006.10:g.32026374G>T	NCBI36
NG_008191.1:g.9675G>T , LRG_136:g.9675G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000452035.7:n.2016G>T
ENST00000483004.2:c.1409-1G>T	ENSP00000419887.2:n.1409-1G>T
ENST00000698628.1:c.1624+215G>T	ENSP00000513848.1:n.1624+215G>T
ENST00000698629.1:n.1802-1G>T
ENST00000698630.1:n.2341-1G>T
ENST00000698631.1:n.2342-1G>T
ENST00000698632.1:n.3135G>T
ENST00000698633.1:n.3025G>T
ENST00000698636.1:n.1847-1G>T
ENST00000425368.7:c.1625-1G>T MANE Select	ENSP00000416561.2:n.1625-1G>T
ENST00000425368.6:c.1625-1G>T	ENSP00000416561.2:n.1625-1G>T
ENST00000452035.6:n.1839G>T
ENST00000456570.5:c.3131-1G>T	ENSP00000410815.1:n.3131-1G>T
ENST00000467360.1:n.750G>T
ENST00000477310.1:c.2678-1G>T	ENSP00000418996.1:n.2678-1G>T
ENST00000483004.1:c.247-1G>T
NM_001710.5:c.1625-1G>T , LRG_136t1:c.1625-1G>T	NP_001701.2:n.1625-1G>T
NM_001710.6:c.1625-1G>T MANE Select	NP_001701.2:n.1625-1G>T