Canonical Allele Identifier: CA2461405483

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541141T= , CM000685.2:g.139541141T=	GRCh38
NC_000023.10:g.138623300T= , CM000685.1:g.138623300T=	GRCh37
NC_000023.9:g.138450966T=	NCBI36
NG_007994.1:g.15406T= , LRG_556:g.15406T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.343T= MANE Select	ENSP00000218099.2:p.Tyr115=
ENST00000218099.6:c.343T=	ENSP00000218099.2:p.Tyr115=
ENST00000394090.2:c.277+3755T=	ENSP00000377650.2:n.277+3755T=
ENST00000479617.2:n.296T=
NM_000133.3:c.343T= , LRG_556t1:c.343T=	NP_000124.1:p.Tyr115=
NM_001313913.1:c.277+3755T=	NP_001300842.1:n.277+3755T=
XM_005262397.3:c.343T=	XP_005262454.1:p.Tyr115=
XM_005262397.4:c.343T=	XP_005262454.1:p.Tyr115=
NM_000133.4:c.343T= MANE Select	NP_000124.1:p.Tyr115=
NM_001313913.2:c.277+3755T=	NP_001300842.1:n.277+3755T=