Canonical Allele Identifier: CA363409296

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918526G>T (hg19) ; chr6:g.31950749G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950749G>T , CM000668.2:g.31950749G>T	GRCh38
NC_000006.11:g.31918526G>T , CM000668.1:g.31918526G>T	GRCh37
NC_000006.10:g.32026505G>T	NCBI36
NG_008191.1:g.9806G>T , LRG_136:g.9806G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2147G>T
ENST00000483004.2:c.1539G>T	ENSP00000419887.2:p.Lys513Asn
ENST00000698628.1:c.1624+346G>T	ENSP00000513848.1:n.1624+346G>T
ENST00000698629.1:n.1932G>T
ENST00000698630.1:n.2471G>T
ENST00000698631.1:n.2472G>T
ENST00000698632.1:n.3266G>T
ENST00000698633.1:n.3156G>T
ENST00000698636.1:n.1977G>T
ENST00000425368.7:c.1755G>T MANE Select	ENSP00000416561.2:p.Lys585Asn
ENST00000425368.6:c.1755G>T	ENSP00000416561.2:p.Lys585Asn
ENST00000456570.5:c.3261G>T	ENSP00000410815.1:p.Lys1087Asn
ENST00000467360.1:n.881G>T
ENST00000477310.1:c.2808G>T	ENSP00000418996.1:p.Lys936Asn
ENST00000483004.1:c.377G>T
NM_001710.5:c.1755G>T , LRG_136t1:c.1755G>T	NP_001701.2:p.Lys585Asn
NM_001710.6:c.1755G>T MANE Select	NP_001701.2:p.Lys585Asn