Canonical Allele Identifier: CA2461412357

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562189T= , CM000685.2:g.139562189T=	GRCh38
NC_000023.10:g.138644348T= , CM000685.1:g.138644348T=	GRCh37
NC_000023.9:g.138472014T=	NCBI36
NG_007994.1:g.36454T= , LRG_556:g.36454T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*118T= MANE Select	ENSP00000218099.2:n.*118T=
ENST00000643157.1:n.1723+448T=
ENST00000218099.6:c.*118T=	ENSP00000218099.2:n.*118T=
NM_000133.3:c.*118T= , LRG_556t1:c.*118T=	NP_000124.1:n.*118T=
NM_001313913.1:c.*118T=	NP_001300842.1:n.*118T=
XM_005262397.3:c.*118T=	XP_005262454.1:n.*118T=
XM_005262397.4:c.*118T=	XP_005262454.1:n.*118T=
NM_000133.4:c.*118T= MANE Select	NP_000124.1:n.*118T=
NM_001313913.2:c.*118T=	NP_001300842.1:n.*118T=