Canonical Allele Identifier: CA2461411821

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560785C= , CM000685.2:g.139560785C=	GRCh38
NC_000023.10:g.138642944C= , CM000685.1:g.138642944C=	GRCh37
NC_000023.9:g.138470610C=	NCBI36
NG_007994.1:g.35050C= , LRG_556:g.35050C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.768C= MANE Select	ENSP00000218099.2:p.Ile256=
ENST00000643157.1:n.1435C=
ENST00000218099.6:c.768C=	ENSP00000218099.2:p.Ile256=
ENST00000394090.2:c.654C=	ENSP00000377650.2:p.Ile218=
NM_000133.3:c.768C= , LRG_556t1:c.768C=	NP_000124.1:p.Ile256=
NM_001313913.1:c.654C=	NP_001300842.1:p.Ile218=
XM_005262397.3:c.639C=	XP_005262454.1:p.Ile213=
XM_005262397.4:c.639C=	XP_005262454.1:p.Ile213=
NM_000133.4:c.768C= MANE Select	NP_000124.1:p.Ile256=
NM_001313913.2:c.654C=	NP_001300842.1:p.Ile218=