Canonical Allele Identifier: CA2461412053

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561480G= , CM000685.2:g.139561480G=	GRCh38
NC_000023.10:g.138643639G= , CM000685.1:g.138643639G=	GRCh37
NC_000023.9:g.138471305G=	NCBI36
NG_007994.1:g.35745G= , LRG_556:g.35745G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.839-44G= MANE Select	ENSP00000218099.2:n.839-44G=
ENST00000643157.1:n.1506-44G=
ENST00000218099.6:c.839-44G=	ENSP00000218099.2:n.839-44G=
ENST00000394090.2:c.725-44G=	ENSP00000377650.2:n.725-44G=
NM_000133.3:c.839-44G= , LRG_556t1:c.839-44G=	NP_000124.1:n.839-44G=
NM_001313913.1:c.725-44G=	NP_001300842.1:n.725-44G=
XM_005262397.3:c.710-44G=	XP_005262454.1:n.710-44G=
XM_005262397.4:c.710-44G=	XP_005262454.1:n.710-44G=
NM_000133.4:c.839-44G= MANE Select	NP_000124.1:n.839-44G=
NM_001313913.2:c.725-44G=	NP_001300842.1:n.725-44G=