Canonical Allele Identifier: CA2461408615

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551154A= , CM000685.2:g.139551154A=	GRCh38
NC_000023.10:g.138633313A= , CM000685.1:g.138633313A=	GRCh37
NC_000023.9:g.138460979A=	NCBI36
NG_007994.1:g.25419A= , LRG_556:g.25419A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.613A= MANE Select	ENSP00000218099.2:p.Thr205=
ENST00000643157.1:n.1280A=
ENST00000218099.6:c.613A=	ENSP00000218099.2:p.Thr205=
ENST00000394090.2:c.499A=	ENSP00000377650.2:p.Thr167=
NM_000133.3:c.613A= , LRG_556t1:c.613A=	NP_000124.1:p.Thr205=
NM_001313913.1:c.499A=	NP_001300842.1:p.Thr167=
XM_005262397.3:c.484A=	XP_005262454.1:p.Thr162=
XM_005262397.4:c.484A=	XP_005262454.1:p.Thr162=
NM_000133.4:c.613A= MANE Select	NP_000124.1:p.Thr205=
NM_001313913.2:c.499A=	NP_001300842.1:p.Thr167=