Canonical Allele Identifier: CA2461408613

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551147A= , CM000685.2:g.139551147A=	GRCh38
NC_000023.10:g.138633306A= , CM000685.1:g.138633306A=	GRCh37
NC_000023.9:g.138460972A=	NCBI36
NG_007994.1:g.25412A= , LRG_556:g.25412A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.606A= MANE Select	ENSP00000218099.2:p.Val202=
ENST00000643157.1:n.1273A=
ENST00000218099.6:c.606A=	ENSP00000218099.2:p.Val202=
ENST00000394090.2:c.492A=	ENSP00000377650.2:p.Val164=
NM_000133.3:c.606A= , LRG_556t1:c.606A=	NP_000124.1:p.Val202=
NM_001313913.1:c.492A=	NP_001300842.1:p.Val164=
XM_005262397.3:c.477A=	XP_005262454.1:p.Val159=
XM_005262397.4:c.477A=	XP_005262454.1:p.Val159=
NM_000133.4:c.606A= MANE Select	NP_000124.1:p.Val202=
NM_001313913.2:c.492A=	NP_001300842.1:p.Val164=