Canonical Allele Identifier: CA2461411847

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560852G= , CM000685.2:g.139560852G=	GRCh38
NC_000023.10:g.138643011G= , CM000685.1:g.138643011G=	GRCh37
NC_000023.9:g.138470677G=	NCBI36
NG_007994.1:g.35117G= , LRG_556:g.35117G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.835G= MANE Select	ENSP00000218099.2:p.Ala279=
ENST00000643157.1:n.1502G=
ENST00000218099.6:c.835G=	ENSP00000218099.2:p.Ala279=
ENST00000394090.2:c.721G=	ENSP00000377650.2:p.Ala241=
NM_000133.3:c.835G= , LRG_556t1:c.835G=	NP_000124.1:p.Ala279=
NM_001313913.1:c.721G=	NP_001300842.1:p.Ala241=
XM_005262397.3:c.706G=	XP_005262454.1:p.Ala236=
XM_005262397.4:c.706G=	XP_005262454.1:p.Ala236=
NM_000133.4:c.835G= MANE Select	NP_000124.1:p.Ala279=
NM_001313913.2:c.721G=	NP_001300842.1:p.Ala241=