Canonical Allele Identifier: CA363388369

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31914237T>C (hg19) ; chr6:g.31946460T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946460T>C , CM000668.2:g.31946460T>C	GRCh38
NC_000006.11:g.31914237T>C , CM000668.1:g.31914237T>C	GRCh37
NC_000006.10:g.32022216T>C	NCBI36
NG_008191.1:g.5517T>C , LRG_136:g.5517T>C
NG_011730.1:g.23972T>C , LRG_26:g.23972T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.329T>C
ENST00000483004.2:c.152T>C	ENSP00000419887.2:p.Leu51Pro
ENST00000497841.6:c.152T>C	ENSP00000513847.1:p.Leu51Pro
ENST00000698628.1:c.152T>C	ENSP00000513848.1:p.Leu51Pro
ENST00000698629.1:n.329T>C
ENST00000698630.1:n.313T>C
ENST00000698631.1:n.308T>C
ENST00000698632.1:n.280T>C
ENST00000698633.1:n.250T>C
ENST00000698636.1:n.374T>C
ENST00000425368.7:c.152T>C MANE Select	ENSP00000416561.2:p.Leu51Pro
ENST00000425368.6:c.152T>C	ENSP00000416561.2:p.Leu51Pro
ENST00000452035.6:n.152T>C
ENST00000456570.5:c.1658T>C	ENSP00000410815.1:p.Leu553Pro
ENST00000460718.5:c.65-26T>C	ENSP00000417793.1:n.65-26T>C
ENST00000472581.1:n.399T>C
ENST00000475617.5:c.152T>C	ENSP00000420090.1:p.Leu51Pro
ENST00000477310.1:c.1352-547T>C	ENSP00000418996.1:n.1352-547T>C
NM_001710.5:c.152T>C , LRG_136t1:c.152T>C	NP_001701.2:p.Leu51Pro
NM_001710.6:c.152T>C MANE Select	NP_001701.2:p.Leu51Pro