Canonical Allele Identifier: CA2461408602

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551113G= , CM000685.2:g.139551113G=	GRCh38
NC_000023.10:g.138633272G= , CM000685.1:g.138633272G=	GRCh37
NC_000023.9:g.138460938G=	NCBI36
NG_007994.1:g.25378G= , LRG_556:g.25378G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.572G= MANE Select	ENSP00000218099.2:p.Arg191=
ENST00000643157.1:n.1239G=
ENST00000218099.6:c.572G=	ENSP00000218099.2:p.Arg191=
ENST00000394090.2:c.458G=	ENSP00000377650.2:p.Arg153=
NM_000133.3:c.572G= , LRG_556t1:c.572G=	NP_000124.1:p.Arg191=
NM_001313913.1:c.458G=	NP_001300842.1:p.Arg153=
XM_005262397.3:c.443G=	XP_005262454.1:p.Arg148=
XM_005262397.4:c.443G=	XP_005262454.1:p.Arg148=
NM_000133.4:c.572G= MANE Select	NP_000124.1:p.Arg191=
NM_001313913.2:c.458G=	NP_001300842.1:p.Arg153=