Canonical Allele Identifier: CA3728473

Gene: CFB

Linked Data

• dbSNP Id: rs146329167
• ExAC: 6:31918872 G / C
• gnomAD v2: 6-31918872-G-C
• gnomAD v3: 6-31951095-G-C
• gnomAD v4: 6-31951095-G-C
• MyVariant Identifiers: chr6:g.31918872G>C (hg19) ; chr6:g.31951095G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951095G>C , CM000668.2:g.31951095G>C	GRCh38
NC_000006.11:g.31918872G>C , CM000668.1:g.31918872G>C	GRCh37
NC_000006.10:g.32026851G>C	NCBI36
NG_008191.1:g.10152G>C , LRG_136:g.10152G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-102G>C
ENST00000483004.2:c.1640-49G>C	ENSP00000419887.2:n.1640-49G>C
ENST00000698628.1:c.1625-49G>C	ENSP00000513848.1:n.1625-49G>C
ENST00000698629.1:n.2128-102G>C
ENST00000698630.1:n.2572-49G>C
ENST00000698631.1:n.2573-49G>C
ENST00000698632.1:n.3612G>C
ENST00000698633.1:n.3502G>C
ENST00000425368.7:c.1856-49G>C MANE Select	ENSP00000416561.2:n.1856-49G>C
ENST00000425368.6:c.1856-49G>C	ENSP00000416561.2:n.1856-49G>C
ENST00000456570.5:c.3362-49G>C	ENSP00000410815.1:n.3362-49G>C
ENST00000467360.1:n.982-49G>C
ENST00000477310.1:c.2909-49G>C	ENSP00000418996.1:n.2909-49G>C
ENST00000482312.1:n.222G>C
ENST00000483004.1:c.478-49G>C
NM_001710.5:c.1856-49G>C , LRG_136t1:c.1856-49G>C	NP_001701.2:n.1856-49G>C
NM_001710.6:c.1856-49G>C MANE Select	NP_001701.2:n.1856-49G>C