Canonical Allele Identifier: CA2461411997

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561289C= , CM000685.2:g.139561289C=	GRCh38
NC_000023.10:g.138643448C= , CM000685.1:g.138643448C=	GRCh37
NC_000023.9:g.138471114C=	NCBI36
NG_007994.1:g.35554C= , LRG_556:g.35554C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.839-235C= MANE Select	ENSP00000218099.2:n.839-235C=
ENST00000643157.1:n.1506-235C=
ENST00000218099.6:c.839-235C=	ENSP00000218099.2:n.839-235C=
ENST00000394090.2:c.725-235C=	ENSP00000377650.2:n.725-235C=
NM_000133.3:c.839-235C= , LRG_556t1:c.839-235C=	NP_000124.1:n.839-235C=
NM_001313913.1:c.725-235C=	NP_001300842.1:n.725-235C=
XM_005262397.3:c.710-235C=	XP_005262454.1:n.710-235C=
XM_005262397.4:c.710-235C=	XP_005262454.1:n.710-235C=
NM_000133.4:c.839-235C= MANE Select	NP_000124.1:n.839-235C=
NM_001313913.2:c.725-235C=	NP_001300842.1:n.725-235C=