Canonical Allele Identifier: CA2461408607

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551123T= , CM000685.2:g.139551123T=	GRCh38
NC_000023.10:g.138633282T= , CM000685.1:g.138633282T=	GRCh37
NC_000023.9:g.138460948T=	NCBI36
NG_007994.1:g.25388T= , LRG_556:g.25388T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.582T= MANE Select	ENSP00000218099.2:p.Thr194=
ENST00000643157.1:n.1249T=
ENST00000218099.6:c.582T=	ENSP00000218099.2:p.Thr194=
ENST00000394090.2:c.468T=	ENSP00000377650.2:p.Thr156=
NM_000133.3:c.582T= , LRG_556t1:c.582T=	NP_000124.1:p.Thr194=
NM_001313913.1:c.468T=	NP_001300842.1:p.Thr156=
XM_005262397.3:c.453T=	XP_005262454.1:p.Thr151=
XM_005262397.4:c.453T=	XP_005262454.1:p.Thr151=
NM_000133.4:c.582T= MANE Select	NP_000124.1:p.Thr194=
NM_001313913.2:c.468T=	NP_001300842.1:p.Thr156=