Canonical Allele Identifier: CA2461411857

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560881C= , CM000685.2:g.139560881C=	GRCh38
NC_000023.10:g.138643040C= , CM000685.1:g.138643040C=	GRCh37
NC_000023.9:g.138470706C=	NCBI36
NG_007994.1:g.35146C= , LRG_556:g.35146C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.838+26C= MANE Select	ENSP00000218099.2:n.838+26C=
ENST00000643157.1:n.1505+26C=
ENST00000218099.6:c.838+26C=	ENSP00000218099.2:n.838+26C=
ENST00000394090.2:c.724+26C=	ENSP00000377650.2:n.724+26C=
NM_000133.3:c.838+26C= , LRG_556t1:c.838+26C=	NP_000124.1:n.838+26C=
NM_001313913.1:c.724+26C=	NP_001300842.1:n.724+26C=
XM_005262397.3:c.709+26C=	XP_005262454.1:n.709+26C=
XM_005262397.4:c.709+26C=	XP_005262454.1:n.709+26C=
NM_000133.4:c.838+26C= MANE Select	NP_000124.1:n.838+26C=
NM_001313913.2:c.724+26C=	NP_001300842.1:n.724+26C=