Canonical Allele Identifier: CA2461412089

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561579A= , CM000685.2:g.139561579A=	GRCh38
NC_000023.10:g.138643738A= , CM000685.1:g.138643738A=	GRCh37
NC_000023.9:g.138471404A=	NCBI36
NG_007994.1:g.35844A= , LRG_556:g.35844A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.894A= MANE Select	ENSP00000218099.2:p.Arg298=
ENST00000643157.1:n.1561A=
ENST00000218099.6:c.894A=	ENSP00000218099.2:p.Arg298=
ENST00000394090.2:c.780A=	ENSP00000377650.2:p.Arg260=
NM_000133.3:c.894A= , LRG_556t1:c.894A=	NP_000124.1:p.Arg298=
NM_001313913.1:c.780A=	NP_001300842.1:p.Arg260=
XM_005262397.3:c.765A=	XP_005262454.1:p.Arg255=
XM_005262397.4:c.765A=	XP_005262454.1:p.Arg255=
NM_000133.4:c.894A= MANE Select	NP_000124.1:p.Arg298=
NM_001313913.2:c.780A=	NP_001300842.1:p.Arg260=