Canonical Allele Identifier: CA3728445

Gene: CFB

Linked Data

• dbSNP Id: rs776433225
• ExAC: 6:31918572 G / A
• gnomAD v2: 6-31918572-G-A
• gnomAD v4: 6-31950795-G-A
• MyVariant Identifiers: chr6:g.31918572G>A (hg19) ; chr6:g.31950795G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950795G>A , CM000668.2:g.31950795G>A	GRCh38
NC_000006.11:g.31918572G>A , CM000668.1:g.31918572G>A	GRCh37
NC_000006.10:g.32026551G>A	NCBI36
NG_008191.1:g.9852G>A , LRG_136:g.9852G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2193G>A
ENST00000483004.2:c.1562+23G>A	ENSP00000419887.2:n.1562+23G>A
ENST00000698628.1:c.1625-349G>A	ENSP00000513848.1:n.1625-349G>A
ENST00000698629.1:n.1978G>A
ENST00000698630.1:n.2494+23G>A
ENST00000698631.1:n.2495+23G>A
ENST00000698632.1:n.3312G>A
ENST00000698633.1:n.3202G>A
ENST00000698636.1:n.2023G>A
ENST00000425368.7:c.1778+23G>A MANE Select	ENSP00000416561.2:n.1778+23G>A
ENST00000425368.6:c.1778+23G>A	ENSP00000416561.2:n.1778+23G>A
ENST00000456570.5:c.3284+23G>A	ENSP00000410815.1:n.3284+23G>A
ENST00000467360.1:n.904+23G>A
ENST00000477310.1:c.2831+23G>A	ENSP00000418996.1:n.2831+23G>A
ENST00000483004.1:c.400+23G>A
NM_001710.5:c.1778+23G>A , LRG_136t1:c.1778+23G>A	NP_001701.2:n.1778+23G>A
NM_001710.6:c.1778+23G>A MANE Select	NP_001701.2:n.1778+23G>A