Canonical Allele Identifier: CA2461407782

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548387G= , CM000685.2:g.139548387G=	GRCh38
NC_000023.10:g.138630546G= , CM000685.1:g.138630546G=	GRCh37
NC_000023.9:g.138458212G=	NCBI36
NG_007994.1:g.22652G= , LRG_556:g.22652G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.416G= MANE Select	ENSP00000218099.2:p.Gly139=
ENST00000643157.1:n.1083G=
ENST00000218099.6:c.416G=	ENSP00000218099.2:p.Gly139=
ENST00000394090.2:c.302G=	ENSP00000377650.2:p.Gly101=
ENST00000479617.2:n.369G=
NM_000133.3:c.416G= , LRG_556t1:c.416G=	NP_000124.1:p.Gly139=
NM_001313913.1:c.302G=	NP_001300842.1:p.Gly101=
XM_005262397.3:c.392-2675G=	XP_005262454.1:n.392-2675G=
XM_005262397.4:c.392-2675G=	XP_005262454.1:n.392-2675G=
NM_000133.4:c.416G= MANE Select	NP_000124.1:p.Gly139=
NM_001313913.2:c.302G=	NP_001300842.1:p.Gly101=