Canonical Allele Identifier: CA2461405468

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541085A= , CM000685.2:g.139541085A=	GRCh38
NC_000023.10:g.138623244A= , CM000685.1:g.138623244A=	GRCh37
NC_000023.9:g.138450910A=	NCBI36
NG_007994.1:g.15350A= , LRG_556:g.15350A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.287A= MANE Select	ENSP00000218099.2:p.Gln96=
ENST00000218099.6:c.287A=	ENSP00000218099.2:p.Gln96=
ENST00000394090.2:c.277+3699A=	ENSP00000377650.2:n.277+3699A=
ENST00000479617.2:n.242-2A=
NM_000133.3:c.287A= , LRG_556t1:c.287A=	NP_000124.1:p.Gln96=
NM_001313913.1:c.277+3699A=	NP_001300842.1:n.277+3699A=
XM_005262397.3:c.287A=	XP_005262454.1:p.Gln96=
XM_005262397.4:c.287A=	XP_005262454.1:p.Gln96=
NM_000133.4:c.287A= MANE Select	NP_000124.1:p.Gln96=
NM_001313913.2:c.277+3699A=	NP_001300842.1:n.277+3699A=