Canonical Allele Identifier: CA2461408639

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551226G= , CM000685.2:g.139551226G=	GRCh38
NC_000023.10:g.138633385G= , CM000685.1:g.138633385G=	GRCh37
NC_000023.9:g.138461051G=	NCBI36
NG_007994.1:g.25491G= , LRG_556:g.25491G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.685G= MANE Select	ENSP00000218099.2:p.Gly229=
ENST00000643157.1:n.1352G=
ENST00000218099.6:c.685G=	ENSP00000218099.2:p.Gly229=
ENST00000394090.2:c.571G=	ENSP00000377650.2:p.Gly191=
NM_000133.3:c.685G= , LRG_556t1:c.685G=	NP_000124.1:p.Gly229=
NM_001313913.1:c.571G=	NP_001300842.1:p.Gly191=
XM_005262397.3:c.556G=	XP_005262454.1:p.Gly186=
XM_005262397.4:c.556G=	XP_005262454.1:p.Gly186=
NM_000133.4:c.685G= MANE Select	NP_000124.1:p.Gly229=
NM_001313913.2:c.571G=	NP_001300842.1:p.Gly191=