Canonical Allele Identifier: CA566693428

Gene: CFB

Linked Data

• dbSNP Id: rs1291767543
• gnomAD v2: 6-31914538-A-T
• gnomAD v3: 6-31946761-A-T
• gnomAD v4: 6-31946761-A-T
• MyVariant Identifiers: chr6:g.31914538A>T (hg19) ; chr6:g.31946761A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946761A>T , CM000668.2:g.31946761A>T	GRCh38
NC_000006.11:g.31914538A>T , CM000668.1:g.31914538A>T	GRCh37
NC_000006.10:g.32022517A>T	NCBI36
NG_008191.1:g.5818A>T , LRG_136:g.5818A>T
NG_011730.1:g.24273A>T , LRG_26:g.24273A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.475+155A>T
ENST00000483004.2:c.298+155A>T	ENSP00000419887.2:n.298+155A>T
ENST00000497841.6:c.298+155A>T	ENSP00000513847.1:n.298+155A>T
ENST00000698628.1:c.298+155A>T	ENSP00000513848.1:n.298+155A>T
ENST00000698629.1:n.475+155A>T
ENST00000698630.1:n.614A>T
ENST00000698631.1:n.609A>T
ENST00000698632.1:n.581A>T
ENST00000698633.1:n.551A>T
ENST00000698636.1:n.520+155A>T
ENST00000425368.7:c.298+155A>T MANE Select	ENSP00000416561.2:n.298+155A>T
ENST00000425368.6:c.298+155A>T	ENSP00000416561.2:n.298+155A>T
ENST00000452035.6:n.298+155A>T
ENST00000456570.5:c.1804+155A>T	ENSP00000410815.1:n.1804+155A>T
ENST00000460718.5:c.185+155A>T	ENSP00000417793.1:n.185+155A>T
ENST00000472581.1:n.700A>T
ENST00000475617.5:c.298+155A>T	ENSP00000420090.1:n.298+155A>T
ENST00000477310.1:c.1352-246A>T	ENSP00000418996.1:n.1352-246A>T
NM_001710.5:c.298+155A>T , LRG_136t1:c.298+155A>T	NP_001701.2:n.298+155A>T
NM_001710.6:c.298+155A>T MANE Select	NP_001701.2:n.298+155A>T