Canonical Allele Identifier: CA2461412208
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561859A= , CM000685.2:g.139561859A= GRCh38
NC_000023.10:g.138644018A= , CM000685.1:g.138644018A= GRCh37
NC_000023.9:g.138471684A= NCBI36
NG_007994.1:g.36124A= , LRG_556:g.36124A=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1174A= MANE Select ENSP00000218099.2:p.Asn392=
ENST00000643157.1:n.1723+118A=
ENST00000218099.6:c.1174A= ENSP00000218099.2:p.Asn392=
ENST00000394090.2:c.1060A= ENSP00000377650.2:p.Asn354=
NM_000133.3:c.1174A= , LRG_556t1:c.1174A= NP_000124.1:p.Asn392=
NM_001313913.1:c.1060A= NP_001300842.1:p.Asn354=
XM_005262397.3:c.1045A= XP_005262454.1:p.Asn349=
XM_005262397.4:c.1045A= XP_005262454.1:p.Asn349=
NM_000133.4:c.1174A= MANE Select NP_000124.1:p.Asn392=
NM_001313913.2:c.1060A= NP_001300842.1:p.Asn354=