Canonical Allele Identifier: CA2461412205
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561855C= , CM000685.2:g.139561855C= GRCh38
NC_000023.10:g.138644014C= , CM000685.1:g.138644014C= GRCh37
NC_000023.9:g.138471680C= NCBI36
NG_007994.1:g.36120C= , LRG_556:g.36120C=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1170C= MANE Select ENSP00000218099.2:p.Ile390=
ENST00000643157.1:n.1723+114C=
ENST00000218099.6:c.1170C= ENSP00000218099.2:p.Ile390=
ENST00000394090.2:c.1056C= ENSP00000377650.2:p.Ile352=
NM_000133.3:c.1170C= , LRG_556t1:c.1170C= NP_000124.1:p.Ile390=
NM_001313913.1:c.1056C= NP_001300842.1:p.Ile352=
XM_005262397.3:c.1041C= XP_005262454.1:p.Ile347=
XM_005262397.4:c.1041C= XP_005262454.1:p.Ile347=
NM_000133.4:c.1170C= MANE Select NP_000124.1:p.Ile390=
NM_001313913.2:c.1056C= NP_001300842.1:p.Ile352=