Canonical Allele Identifier: CA823922683

Gene: CFB

Linked Data

• dbSNP Id: rs1261479558
• MyVariant Identifiers: chr6:g.31918226G>C (hg19) ; chr6:g.31950449G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950449G>C , CM000668.2:g.31950449G>C	GRCh38
NC_000006.11:g.31918226G>C , CM000668.1:g.31918226G>C	GRCh37
NC_000006.10:g.32026205G>C	NCBI36
NG_008191.1:g.9506G>C , LRG_136:g.9506G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.1847G>C
ENST00000483004.2:c.1409-170G>C	ENSP00000419887.2:n.1409-170G>C
ENST00000698628.1:c.1624+46G>C	ENSP00000513848.1:n.1624+46G>C
ENST00000698629.1:n.1801+46G>C
ENST00000698630.1:n.2340+46G>C
ENST00000698631.1:n.2341+46G>C
ENST00000698632.1:n.2966G>C
ENST00000698633.1:n.2856G>C
ENST00000698636.1:n.1846+46G>C
ENST00000425368.7:c.1624+46G>C MANE Select	ENSP00000416561.2:n.1624+46G>C
ENST00000425368.6:c.1624+46G>C	ENSP00000416561.2:n.1624+46G>C
ENST00000452035.6:n.1670G>C
ENST00000456570.5:c.3130+46G>C	ENSP00000410815.1:n.3130+46G>C
ENST00000467360.1:n.581G>C
ENST00000477310.1:c.2677+46G>C	ENSP00000418996.1:n.2677+46G>C
ENST00000483004.1:c.247-170G>C
NM_001710.5:c.1624+46G>C , LRG_136t1:c.1624+46G>C	NP_001701.2:n.1624+46G>C
NM_001710.6:c.1624+46G>C MANE Select	NP_001701.2:n.1624+46G>C