Canonical Allele Identifier: CA2461412368

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562226G= , CM000685.2:g.139562226G=	GRCh38
NC_000023.10:g.138644385G= , CM000685.1:g.138644385G=	GRCh37
NC_000023.9:g.138472051G=	NCBI36
NG_007994.1:g.36491G= , LRG_556:g.36491G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*155G= MANE Select	ENSP00000218099.2:n.*155G=
ENST00000643157.1:n.1723+485G=
ENST00000218099.6:c.*155G=	ENSP00000218099.2:n.*155G=
NM_000133.3:c.*155G= , LRG_556t1:c.*155G=	NP_000124.1:n.*155G=
NM_001313913.1:c.*155G=	NP_001300842.1:n.*155G=
XM_005262397.3:c.*155G=	XP_005262454.1:n.*155G=
XM_005262397.4:c.*155G=	XP_005262454.1:n.*155G=
NM_000133.4:c.*155G= MANE Select	NP_000124.1:n.*155G=
NM_001313913.2:c.*155G=	NP_001300842.1:n.*155G=