Canonical Allele Identifier: CA2461408632

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551215C= , CM000685.2:g.139551215C=	GRCh38
NC_000023.10:g.138633374C= , CM000685.1:g.138633374C=	GRCh37
NC_000023.9:g.138461040C=	NCBI36
NG_007994.1:g.25480C= , LRG_556:g.25480C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.674C= MANE Select	ENSP00000218099.2:p.Thr225=
ENST00000643157.1:n.1341C=
ENST00000218099.6:c.674C=	ENSP00000218099.2:p.Thr225=
ENST00000394090.2:c.560C=	ENSP00000377650.2:p.Thr187=
NM_000133.3:c.674C= , LRG_556t1:c.674C=	NP_000124.1:p.Thr225=
NM_001313913.1:c.560C=	NP_001300842.1:p.Thr187=
XM_005262397.3:c.545C=	XP_005262454.1:p.Thr182=
XM_005262397.4:c.545C=	XP_005262454.1:p.Thr182=
NM_000133.4:c.674C= MANE Select	NP_000124.1:p.Thr225=
NM_001313913.2:c.560C=	NP_001300842.1:p.Thr187=