Canonical Allele Identifier: CA2461412138

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561710C= , CM000685.2:g.139561710C=	GRCh38
NC_000023.10:g.138643869C= , CM000685.1:g.138643869C=	GRCh37
NC_000023.9:g.138471535C=	NCBI36
NG_007994.1:g.35975C= , LRG_556:g.35975C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1025C= MANE Select	ENSP00000218099.2:p.Thr342=
ENST00000643157.1:n.1692C=
ENST00000218099.6:c.1025C=	ENSP00000218099.2:p.Thr342=
ENST00000394090.2:c.911C=	ENSP00000377650.2:p.Thr304=
NM_000133.3:c.1025C= , LRG_556t1:c.1025C=	NP_000124.1:p.Thr342=
NM_001313913.1:c.911C=	NP_001300842.1:p.Thr304=
XM_005262397.3:c.896C=	XP_005262454.1:p.Thr299=
XM_005262397.4:c.896C=	XP_005262454.1:p.Thr299=
NM_000133.4:c.1025C= MANE Select	NP_000124.1:p.Thr342=
NM_001313913.2:c.911C=	NP_001300842.1:p.Thr304=