Canonical Allele Identifier: CA2461408631

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551211T= , CM000685.2:g.139551211T=	GRCh38
NC_000023.10:g.138633370T= , CM000685.1:g.138633370T=	GRCh37
NC_000023.9:g.138461036T=	NCBI36
NG_007994.1:g.25476T= , LRG_556:g.25476T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.670T= MANE Select	ENSP00000218099.2:p.Phe224=
ENST00000643157.1:n.1337T=
ENST00000218099.6:c.670T=	ENSP00000218099.2:p.Phe224=
ENST00000394090.2:c.556T=	ENSP00000377650.2:p.Phe186=
NM_000133.3:c.670T= , LRG_556t1:c.670T=	NP_000124.1:p.Phe224=
NM_001313913.1:c.556T=	NP_001300842.1:p.Phe186=
XM_005262397.3:c.541T=	XP_005262454.1:p.Phe181=
XM_005262397.4:c.541T=	XP_005262454.1:p.Phe181=
NM_000133.4:c.670T= MANE Select	NP_000124.1:p.Phe224=
NM_001313913.2:c.556T=	NP_001300842.1:p.Phe186=