Canonical Allele Identifier: CA2461412203
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561853A= , CM000685.2:g.139561853A= GRCh38
NC_000023.10:g.138644012A= , CM000685.1:g.138644012A= GRCh37
NC_000023.9:g.138471678A= NCBI36
NG_007994.1:g.36118A= , LRG_556:g.36118A=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1168A= MANE Select ENSP00000218099.2:p.Ile390=
ENST00000643157.1:n.1723+112A=
ENST00000218099.6:c.1168A= ENSP00000218099.2:p.Ile390=
ENST00000394090.2:c.1054A= ENSP00000377650.2:p.Ile352=
NM_000133.3:c.1168A= , LRG_556t1:c.1168A= NP_000124.1:p.Ile390=
NM_001313913.1:c.1054A= NP_001300842.1:p.Ile352=
XM_005262397.3:c.1039A= XP_005262454.1:p.Ile347=
XM_005262397.4:c.1039A= XP_005262454.1:p.Ile347=
NM_000133.4:c.1168A= MANE Select NP_000124.1:p.Ile390=
NM_001313913.2:c.1054A= NP_001300842.1:p.Ile352=