Canonical Allele Identifier: CA136897365

Gene: CFB

Linked Data

• dbSNP Id: rs890408661
• MyVariant Identifiers: chr6:g.31918239C>T (hg19) ; chr6:g.31950462C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950462C>T , CM000668.2:g.31950462C>T	GRCh38
NC_000006.11:g.31918239C>T , CM000668.1:g.31918239C>T	GRCh37
NC_000006.10:g.32026218C>T	NCBI36
NG_008191.1:g.9519C>T , LRG_136:g.9519C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.1860C>T
ENST00000483004.2:c.1409-157C>T	ENSP00000419887.2:n.1409-157C>T
ENST00000698628.1:c.1624+59C>T	ENSP00000513848.1:n.1624+59C>T
ENST00000698629.1:n.1801+59C>T
ENST00000698630.1:n.2340+59C>T
ENST00000698631.1:n.2341+59C>T
ENST00000698632.1:n.2979C>T
ENST00000698633.1:n.2869C>T
ENST00000698636.1:n.1846+59C>T
ENST00000425368.7:c.1624+59C>T MANE Select	ENSP00000416561.2:n.1624+59C>T
ENST00000425368.6:c.1624+59C>T	ENSP00000416561.2:n.1624+59C>T
ENST00000452035.6:n.1683C>T
ENST00000456570.5:c.3130+59C>T	ENSP00000410815.1:n.3130+59C>T
ENST00000467360.1:n.594C>T
ENST00000477310.1:c.2677+59C>T	ENSP00000418996.1:n.2677+59C>T
ENST00000483004.1:c.247-157C>T
NM_001710.5:c.1624+59C>T , LRG_136t1:c.1624+59C>T	NP_001701.2:n.1624+59C>T
NM_001710.6:c.1624+59C>T MANE Select	NP_001701.2:n.1624+59C>T