Canonical Allele Identifier: CA2461408626

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551188A= , CM000685.2:g.139551188A=	GRCh38
NC_000023.10:g.138633347A= , CM000685.1:g.138633347A=	GRCh37
NC_000023.9:g.138461013A=	NCBI36
NG_007994.1:g.25453A= , LRG_556:g.25453A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.647A= MANE Select	ENSP00000218099.2:p.Gln216=
ENST00000643157.1:n.1314A=
ENST00000218099.6:c.647A=	ENSP00000218099.2:p.Gln216=
ENST00000394090.2:c.533A=	ENSP00000377650.2:p.Gln178=
NM_000133.3:c.647A= , LRG_556t1:c.647A=	NP_000124.1:p.Gln216=
NM_001313913.1:c.533A=	NP_001300842.1:p.Gln178=
XM_005262397.3:c.518A=	XP_005262454.1:p.Gln173=
XM_005262397.4:c.518A=	XP_005262454.1:p.Gln173=
NM_000133.4:c.647A= MANE Select	NP_000124.1:p.Gln216=
NM_001313913.2:c.533A=	NP_001300842.1:p.Gln178=