Canonical Allele Identifier: CA2461412099

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561612T= , CM000685.2:g.139561612T=	GRCh38
NC_000023.10:g.138643771T= , CM000685.1:g.138643771T=	GRCh37
NC_000023.9:g.138471437T=	NCBI36
NG_007994.1:g.35877T= , LRG_556:g.35877T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.927T= MANE Select	ENSP00000218099.2:p.Ile309=
ENST00000643157.1:n.1594T=
ENST00000218099.6:c.927T=	ENSP00000218099.2:p.Ile309=
ENST00000394090.2:c.813T=	ENSP00000377650.2:p.Ile271=
NM_000133.3:c.927T= , LRG_556t1:c.927T=	NP_000124.1:p.Ile309=
NM_001313913.1:c.813T=	NP_001300842.1:p.Ile271=
XM_005262397.3:c.798T=	XP_005262454.1:p.Ile266=
XM_005262397.4:c.798T=	XP_005262454.1:p.Ile266=
NM_000133.4:c.927T= MANE Select	NP_000124.1:p.Ile309=
NM_001313913.2:c.813T=	NP_001300842.1:p.Ile271=