Canonical Allele Identifier: CA363387815

Gene: CFB

Linked Data

• gnomAD v4: 6-31946387-C-T
• MyVariant Identifiers: chr6:g.31914164C>T (hg19) ; chr6:g.31946387C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946387C>T , CM000668.2:g.31946387C>T	GRCh38
NC_000006.11:g.31914164C>T , CM000668.1:g.31914164C>T	GRCh37
NC_000006.10:g.32022143C>T	NCBI36
NG_008191.1:g.5444C>T , LRG_136:g.5444C>T
NG_011730.1:g.23899C>T , LRG_26:g.23899C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.256C>T
ENST00000483004.2:c.79C>T	ENSP00000419887.2:p.Pro27Ser
ENST00000497841.6:c.79C>T	ENSP00000513847.1:p.Pro27Ser
ENST00000698628.1:c.79C>T	ENSP00000513848.1:p.Pro27Ser
ENST00000698629.1:n.256C>T
ENST00000698630.1:n.240C>T
ENST00000698631.1:n.235C>T
ENST00000698632.1:n.207C>T
ENST00000698633.1:n.177C>T
ENST00000698636.1:n.301C>T
ENST00000425368.7:c.79C>T MANE Select	ENSP00000416561.2:p.Pro27Ser
ENST00000425368.6:c.79C>T	ENSP00000416561.2:p.Pro27Ser
ENST00000452035.6:n.79C>T
ENST00000456570.5:c.1585C>T	ENSP00000410815.1:p.Pro529Ser
ENST00000460718.5:c.65-99C>T	ENSP00000417793.1:n.65-99C>T
ENST00000472581.1:n.326C>T
ENST00000475617.5:c.79C>T	ENSP00000420090.1:p.Pro27Ser
ENST00000477310.1:c.1352-620C>T	ENSP00000418996.1:n.1352-620C>T
NM_001710.5:c.79C>T , LRG_136t1:c.79C>T	NP_001701.2:p.Pro27Ser
NM_001710.6:c.79C>T MANE Select	NP_001701.2:p.Pro27Ser