Canonical Allele Identifier: CA2461411852

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560864A= , CM000685.2:g.139560864A=	GRCh38
NC_000023.10:g.138643023A= , CM000685.1:g.138643023A=	GRCh37
NC_000023.9:g.138470689A=	NCBI36
NG_007994.1:g.35129A= , LRG_556:g.35129A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.838+9A= MANE Select	ENSP00000218099.2:n.838+9A=
ENST00000643157.1:n.1505+9A=
ENST00000218099.6:c.838+9A=	ENSP00000218099.2:n.838+9A=
ENST00000394090.2:c.724+9A=	ENSP00000377650.2:n.724+9A=
NM_000133.3:c.838+9A= , LRG_556t1:c.838+9A=	NP_000124.1:n.838+9A=
NM_001313913.1:c.724+9A=	NP_001300842.1:n.724+9A=
XM_005262397.3:c.709+9A=	XP_005262454.1:n.709+9A=
XM_005262397.4:c.709+9A=	XP_005262454.1:n.709+9A=
NM_000133.4:c.838+9A= MANE Select	NP_000124.1:n.838+9A=
NM_001313913.2:c.724+9A=	NP_001300842.1:n.724+9A=