Canonical Allele Identifier: CA11656358
Gene: CFI HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10033900

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109737911T>C , CM000666.2:g.109737911T>C GRCh38
NC_000004.11:g.110659067T>C , CM000666.1:g.110659067T>C GRCh37
NC_000004.10:g.110878516T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011531920.1:c.1558+4580A>G XP_011530222.1:p.=
XM_011531920.2:c.1558+4580A>G XP_011530222.1:p.=
XM_017008164.2:c.1534+4580A>G XP_016863653.1:p.=
XM_017008165.2:c.1513+4580A>G XP_016863654.1:p.=
XM_017008166.2:c.1535-3111A>G XP_016863655.1:p.=