Canonical Allele Identifier: CA2461407813

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548467A= , CM000685.2:g.139548467A=	GRCh38
NC_000023.10:g.138630626A= , CM000685.1:g.138630626A=	GRCh37
NC_000023.9:g.138458292A=	NCBI36
NG_007994.1:g.22732A= , LRG_556:g.22732A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.496A= MANE Select	ENSP00000218099.2:p.Asn166=
ENST00000643157.1:n.1163A=
ENST00000218099.6:c.496A=	ENSP00000218099.2:p.Asn166=
ENST00000394090.2:c.382A=	ENSP00000377650.2:p.Asn128=
NM_000133.3:c.496A= , LRG_556t1:c.496A=	NP_000124.1:p.Asn166=
NM_001313913.1:c.382A=	NP_001300842.1:p.Asn128=
XM_005262397.3:c.392-2595A=	XP_005262454.1:n.392-2595A=
XM_005262397.4:c.392-2595A=	XP_005262454.1:n.392-2595A=
NM_000133.4:c.496A= MANE Select	NP_000124.1:p.Asn166=
NM_001313913.2:c.382A=	NP_001300842.1:p.Asn128=