Canonical Allele Identifier: CA2461411842

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560832G= , CM000685.2:g.139560832G=	GRCh38
NC_000023.10:g.138642991G= , CM000685.1:g.138642991G=	GRCh37
NC_000023.9:g.138470657G=	NCBI36
NG_007994.1:g.35097G= , LRG_556:g.35097G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.815G= MANE Select	ENSP00000218099.2:p.Gly272=
ENST00000643157.1:n.1482G=
ENST00000218099.6:c.815G=	ENSP00000218099.2:p.Gly272=
ENST00000394090.2:c.701G=	ENSP00000377650.2:p.Gly234=
NM_000133.3:c.815G= , LRG_556t1:c.815G=	NP_000124.1:p.Gly272=
NM_001313913.1:c.701G=	NP_001300842.1:p.Gly234=
XM_005262397.3:c.686G=	XP_005262454.1:p.Gly229=
XM_005262397.4:c.686G=	XP_005262454.1:p.Gly229=
NM_000133.4:c.815G= MANE Select	NP_000124.1:p.Gly272=
NM_001313913.2:c.701G=	NP_001300842.1:p.Gly234=