Canonical Allele Identifier: CA2461405471

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541095C= , CM000685.2:g.139541095C=	GRCh38
NC_000023.10:g.138623254C= , CM000685.1:g.138623254C=	GRCh37
NC_000023.9:g.138450920C=	NCBI36
NG_007994.1:g.15360C= , LRG_556:g.15360C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.297C= MANE Select	ENSP00000218099.2:p.Ser99=
ENST00000218099.6:c.297C=	ENSP00000218099.2:p.Ser99=
ENST00000394090.2:c.277+3709C=	ENSP00000377650.2:n.277+3709C=
ENST00000479617.2:n.250C=
NM_000133.3:c.297C= , LRG_556t1:c.297C=	NP_000124.1:p.Ser99=
NM_001313913.1:c.277+3709C=	NP_001300842.1:n.277+3709C=
XM_005262397.3:c.297C=	XP_005262454.1:p.Ser99=
XM_005262397.4:c.297C=	XP_005262454.1:p.Ser99=
NM_000133.4:c.297C= MANE Select	NP_000124.1:p.Ser99=
NM_001313913.2:c.277+3709C=	NP_001300842.1:n.277+3709C=