Canonical Allele Identifier: CA2461408611

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551136G= , CM000685.2:g.139551136G=	GRCh38
NC_000023.10:g.138633295G= , CM000685.1:g.138633295G=	GRCh37
NC_000023.9:g.138460961G=	NCBI36
NG_007994.1:g.25401G= , LRG_556:g.25401G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.595G= MANE Select	ENSP00000218099.2:p.Val199=
ENST00000643157.1:n.1262G=
ENST00000218099.6:c.595G=	ENSP00000218099.2:p.Val199=
ENST00000394090.2:c.481G=	ENSP00000377650.2:p.Val161=
NM_000133.3:c.595G= , LRG_556t1:c.595G=	NP_000124.1:p.Val199=
NM_001313913.1:c.481G=	NP_001300842.1:p.Val161=
XM_005262397.3:c.466G=	XP_005262454.1:p.Val156=
XM_005262397.4:c.466G=	XP_005262454.1:p.Val156=
NM_000133.4:c.595G= MANE Select	NP_000124.1:p.Val199=
NM_001313913.2:c.481G=	NP_001300842.1:p.Val161=