Canonical Allele Identifier: CA3728385

Gene: CFB

Linked Data

• dbSNP Id: rs761579910
• ExAC: 6:31918216 T / C
• gnomAD v2: 6-31918216-T-C
• gnomAD v4: 6-31950439-T-C
• MyVariant Identifiers: chr6:g.31918216T>C (hg19) ; chr6:g.31950439T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950439T>C , CM000668.2:g.31950439T>C	GRCh38
NC_000006.11:g.31918216T>C , CM000668.1:g.31918216T>C	GRCh37
NC_000006.10:g.32026195T>C	NCBI36
NG_008191.1:g.9496T>C , LRG_136:g.9496T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.1837T>C
ENST00000483004.2:c.1409-180T>C	ENSP00000419887.2:n.1409-180T>C
ENST00000698628.1:c.1624+36T>C	ENSP00000513848.1:n.1624+36T>C
ENST00000698629.1:n.1801+36T>C
ENST00000698630.1:n.2340+36T>C
ENST00000698631.1:n.2341+36T>C
ENST00000698632.1:n.2956T>C
ENST00000698633.1:n.2846T>C
ENST00000698636.1:n.1846+36T>C
ENST00000425368.7:c.1624+36T>C MANE Select	ENSP00000416561.2:n.1624+36T>C
ENST00000425368.6:c.1624+36T>C	ENSP00000416561.2:n.1624+36T>C
ENST00000452035.6:n.1660T>C
ENST00000456570.5:c.3130+36T>C	ENSP00000410815.1:n.3130+36T>C
ENST00000467360.1:n.571T>C
ENST00000477310.1:c.2677+36T>C	ENSP00000418996.1:n.2677+36T>C
ENST00000483004.1:c.247-180T>C
NM_001710.5:c.1624+36T>C , LRG_136t1:c.1624+36T>C	NP_001701.2:n.1624+36T>C
NM_001710.6:c.1624+36T>C MANE Select	NP_001701.2:n.1624+36T>C