Canonical Allele Identifier: CA2461407803

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548442T= , CM000685.2:g.139548442T=	GRCh38
NC_000023.10:g.138630601T= , CM000685.1:g.138630601T=	GRCh37
NC_000023.9:g.138458267T=	NCBI36
NG_007994.1:g.22707T= , LRG_556:g.22707T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.471T= MANE Select	ENSP00000218099.2:p.Cys157=
ENST00000643157.1:n.1138T=
ENST00000218099.6:c.471T=	ENSP00000218099.2:p.Cys157=
ENST00000394090.2:c.357T=	ENSP00000377650.2:p.Cys119=
NM_000133.3:c.471T= , LRG_556t1:c.471T=	NP_000124.1:p.Cys157=
NM_001313913.1:c.357T=	NP_001300842.1:p.Cys119=
XM_005262397.3:c.392-2620T=	XP_005262454.1:n.392-2620T=
XM_005262397.4:c.392-2620T=	XP_005262454.1:n.392-2620T=
NM_000133.4:c.471T= MANE Select	NP_000124.1:p.Cys157=
NM_001313913.2:c.357T=	NP_001300842.1:p.Cys119=