Canonical Allele Identifier: CA2461407754

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548329A= , CM000685.2:g.139548329A=	GRCh38
NC_000023.10:g.138630488A= , CM000685.1:g.138630488A=	GRCh37
NC_000023.9:g.138458154A=	NCBI36
NG_007994.1:g.22594A= , LRG_556:g.22594A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-34A= MANE Select	ENSP00000218099.2:n.392-34A=
ENST00000643157.1:n.1059-34A=
ENST00000218099.6:c.392-34A=	ENSP00000218099.2:n.392-34A=
ENST00000394090.2:c.278-34A=	ENSP00000377650.2:n.278-34A=
ENST00000479617.2:n.345-34A=
NM_000133.3:c.392-34A= , LRG_556t1:c.392-34A=	NP_000124.1:n.392-34A=
NM_001313913.1:c.278-34A=	NP_001300842.1:n.278-34A=
XM_005262397.3:c.392-2733A=	XP_005262454.1:n.392-2733A=
XM_005262397.4:c.392-2733A=	XP_005262454.1:n.392-2733A=
NM_000133.4:c.392-34A= MANE Select	NP_000124.1:n.392-34A=
NM_001313913.2:c.278-34A=	NP_001300842.1:n.278-34A=