Canonical Allele Identifier: CA2461408604
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551116C= , CM000685.2:g.139551116C= GRCh38
NC_000023.10:g.138633275C= , CM000685.1:g.138633275C= GRCh37
NC_000023.9:g.138460941C= NCBI36
NG_007994.1:g.25381C= , LRG_556:g.25381C=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.575C= MANE Select ENSP00000218099.2:p.Ala192=
ENST00000643157.1:n.1242C=
ENST00000218099.6:c.575C= ENSP00000218099.2:p.Ala192=
ENST00000394090.2:c.461C= ENSP00000377650.2:p.Ala154=
NM_000133.3:c.575C= , LRG_556t1:c.575C= NP_000124.1:p.Ala192=
NM_001313913.1:c.461C= NP_001300842.1:p.Ala154=
XM_005262397.3:c.446C= XP_005262454.1:p.Ala149=
XM_005262397.4:c.446C= XP_005262454.1:p.Ala149=
NM_000133.4:c.575C= MANE Select NP_000124.1:p.Ala192=
NM_001313913.2:c.461C= NP_001300842.1:p.Ala154=