Canonical Allele Identifier: CA3728427

Gene: CFB

Linked Data

• dbSNP Id: rs776382264
• ExAC: 6:31918437 C / T
• gnomAD v2: 6-31918437-C-T
• MyVariant Identifiers: chr6:g.31918437C>T (hg19) ; chr6:g.31950660C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950660C>T , CM000668.2:g.31950660C>T	GRCh38
NC_000006.11:g.31918437C>T , CM000668.1:g.31918437C>T	GRCh37
NC_000006.10:g.32026416C>T	NCBI36
NG_008191.1:g.9717C>T , LRG_136:g.9717C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2058C>T
ENST00000483004.2:c.1450C>T	ENSP00000419887.2:p.His484Tyr
ENST00000698628.1:c.1624+257C>T	ENSP00000513848.1:n.1624+257C>T
ENST00000698629.1:n.1843C>T
ENST00000698630.1:n.2382C>T
ENST00000698631.1:n.2383C>T
ENST00000698632.1:n.3177C>T
ENST00000698633.1:n.3067C>T
ENST00000698636.1:n.1888C>T
ENST00000425368.7:c.1666C>T MANE Select	ENSP00000416561.2:p.His556Tyr
ENST00000425368.6:c.1666C>T	ENSP00000416561.2:p.His556Tyr
ENST00000456570.5:c.3172C>T	ENSP00000410815.1:p.His1058Tyr
ENST00000467360.1:n.792C>T
ENST00000477310.1:c.2719C>T	ENSP00000418996.1:p.His907Tyr
ENST00000483004.1:c.288C>T
NM_001710.5:c.1666C>T , LRG_136t1:c.1666C>T	NP_001701.2:p.His556Tyr
NM_001710.6:c.1666C>T MANE Select	NP_001701.2:p.His556Tyr