Canonical Allele Identifier: CA2461411838

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560825G= , CM000685.2:g.139560825G=	GRCh38
NC_000023.10:g.138642984G= , CM000685.1:g.138642984G=	GRCh37
NC_000023.9:g.138470650G=	NCBI36
NG_007994.1:g.35090G= , LRG_556:g.35090G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.808G= MANE Select	ENSP00000218099.2:p.Glu270=
ENST00000643157.1:n.1475G=
ENST00000218099.6:c.808G=	ENSP00000218099.2:p.Glu270=
ENST00000394090.2:c.694G=	ENSP00000377650.2:p.Glu232=
NM_000133.3:c.808G= , LRG_556t1:c.808G=	NP_000124.1:p.Glu270=
NM_001313913.1:c.694G=	NP_001300842.1:p.Glu232=
XM_005262397.3:c.679G=	XP_005262454.1:p.Glu227=
XM_005262397.4:c.679G=	XP_005262454.1:p.Glu227=
NM_000133.4:c.808G= MANE Select	NP_000124.1:p.Glu270=
NM_001313913.2:c.694G=	NP_001300842.1:p.Glu232=