Canonical Allele Identifier: CA2461412097

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561602A= , CM000685.2:g.139561602A=	GRCh38
NC_000023.10:g.138643761A= , CM000685.1:g.138643761A=	GRCh37
NC_000023.9:g.138471427A=	NCBI36
NG_007994.1:g.35867A= , LRG_556:g.35867A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.917A= MANE Select	ENSP00000218099.2:p.Asn306=
ENST00000643157.1:n.1584A=
ENST00000218099.6:c.917A=	ENSP00000218099.2:p.Asn306=
ENST00000394090.2:c.803A=	ENSP00000377650.2:p.Asn268=
NM_000133.3:c.917A= , LRG_556t1:c.917A=	NP_000124.1:p.Asn306=
NM_001313913.1:c.803A=	NP_001300842.1:p.Asn268=
XM_005262397.3:c.788A=	XP_005262454.1:p.Asn263=
XM_005262397.4:c.788A=	XP_005262454.1:p.Asn263=
NM_000133.4:c.917A= MANE Select	NP_000124.1:p.Asn306=
NM_001313913.2:c.803A=	NP_001300842.1:p.Asn268=