Canonical Allele Identifier: CA363389589

Gene: CFB

Linked Data

• dbSNP Id: rs1771436539
• gnomAD v3: 6-31946572-A-T
• gnomAD v4: 6-31946572-A-T
• MyVariant Identifiers: chr6:g.31914349A>T (hg19) ; chr6:g.31946572A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946572A>T , CM000668.2:g.31946572A>T	GRCh38
NC_000006.11:g.31914349A>T , CM000668.1:g.31914349A>T	GRCh37
NC_000006.10:g.32022328A>T	NCBI36
NG_008191.1:g.5629A>T , LRG_136:g.5629A>T
NG_011730.1:g.24084A>T , LRG_26:g.24084A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.441A>T
ENST00000483004.2:c.264A>T	ENSP00000419887.2:p.Gln88His
ENST00000497841.6:c.264A>T	ENSP00000513847.1:p.Gln88His
ENST00000698628.1:c.264A>T	ENSP00000513848.1:p.Gln88His
ENST00000698629.1:n.441A>T
ENST00000698630.1:n.425A>T
ENST00000698631.1:n.420A>T
ENST00000698632.1:n.392A>T
ENST00000698633.1:n.362A>T
ENST00000698636.1:n.486A>T
ENST00000425368.7:c.264A>T MANE Select	ENSP00000416561.2:p.Gln88His
ENST00000425368.6:c.264A>T	ENSP00000416561.2:p.Gln88His
ENST00000452035.6:n.264A>T
ENST00000456570.5:c.1770A>T	ENSP00000410815.1:p.Gln590His
ENST00000460718.5:c.151A>T	ENSP00000417793.1:p.Arg51Ter
ENST00000472581.1:n.511A>T
ENST00000475617.5:c.264A>T	ENSP00000420090.1:p.Gln88His
ENST00000477310.1:c.1352-435A>T	ENSP00000418996.1:n.1352-435A>T
NM_001710.5:c.264A>T , LRG_136t1:c.264A>T	NP_001701.2:p.Gln88His
NM_001710.6:c.264A>T MANE Select	NP_001701.2:p.Gln88His