Canonical Allele Identifier: CA2461408601
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551112C= , CM000685.2:g.139551112C= GRCh38
NC_000023.10:g.138633271C= , CM000685.1:g.138633271C= GRCh37
NC_000023.9:g.138460937C= NCBI36
NG_007994.1:g.25377C= , LRG_556:g.25377C=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.571C= MANE Select ENSP00000218099.2:p.Arg191=
ENST00000643157.1:n.1238C=
ENST00000218099.6:c.571C= ENSP00000218099.2:p.Arg191=
ENST00000394090.2:c.457C= ENSP00000377650.2:p.Arg153=
NM_000133.3:c.571C= , LRG_556t1:c.571C= NP_000124.1:p.Arg191=
NM_001313913.1:c.457C= NP_001300842.1:p.Arg153=
XM_005262397.3:c.442C= XP_005262454.1:p.Arg148=
XM_005262397.4:c.442C= XP_005262454.1:p.Arg148=
NM_000133.4:c.571C= MANE Select NP_000124.1:p.Arg191=
NM_001313913.2:c.457C= NP_001300842.1:p.Arg153=