Canonical Allele Identifier: CA2461408638

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551225T= , CM000685.2:g.139551225T=	GRCh38
NC_000023.10:g.138633384T= , CM000685.1:g.138633384T=	GRCh37
NC_000023.9:g.138461050T=	NCBI36
NG_007994.1:g.25490T= , LRG_556:g.25490T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.684T= MANE Select	ENSP00000218099.2:p.Val228=
ENST00000643157.1:n.1351T=
ENST00000218099.6:c.684T=	ENSP00000218099.2:p.Val228=
ENST00000394090.2:c.570T=	ENSP00000377650.2:p.Val190=
NM_000133.3:c.684T= , LRG_556t1:c.684T=	NP_000124.1:p.Val228=
NM_001313913.1:c.570T=	NP_001300842.1:p.Val190=
XM_005262397.3:c.555T=	XP_005262454.1:p.Val185=
XM_005262397.4:c.555T=	XP_005262454.1:p.Val185=
NM_000133.4:c.684T= MANE Select	NP_000124.1:p.Val228=
NM_001313913.2:c.570T=	NP_001300842.1:p.Val190=