Canonical Allele Identifier: CA2461405490

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541162G= , CM000685.2:g.139541162G=	GRCh38
NC_000023.10:g.138623321G= , CM000685.1:g.138623321G=	GRCh37
NC_000023.9:g.138450987G=	NCBI36
NG_007994.1:g.15427G= , LRG_556:g.15427G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.364G= MANE Select	ENSP00000218099.2:p.Gly122=
ENST00000218099.6:c.364G=	ENSP00000218099.2:p.Gly122=
ENST00000394090.2:c.277+3776G=	ENSP00000377650.2:n.277+3776G=
ENST00000479617.2:n.317G=
NM_000133.3:c.364G= , LRG_556t1:c.364G=	NP_000124.1:p.Gly122=
NM_001313913.1:c.277+3776G=	NP_001300842.1:n.277+3776G=
XM_005262397.3:c.364G=	XP_005262454.1:p.Gly122=
XM_005262397.4:c.364G=	XP_005262454.1:p.Gly122=
NM_000133.4:c.364G= MANE Select	NP_000124.1:p.Gly122=
NM_001313913.2:c.277+3776G=	NP_001300842.1:n.277+3776G=