Canonical Allele Identifier: CA2461404316

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537152T= , CM000685.2:g.139537152T=	GRCh38
NC_000023.10:g.138619311T= , CM000685.1:g.138619311T=	GRCh37
NC_000023.9:g.138446977T=	NCBI36
NG_007994.1:g.11417T= , LRG_556:g.11417T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.231T= MANE Select	ENSP00000218099.2:p.Val77=
ENST00000218099.6:c.231T=	ENSP00000218099.2:p.Val77=
ENST00000394090.2:c.231T=	ENSP00000377650.2:p.Val77=
ENST00000479617.2:n.238T=
NM_000133.3:c.231T= , LRG_556t1:c.231T=	NP_000124.1:p.Val77=
NM_001313913.1:c.231T=	NP_001300842.1:p.Val77=
XM_005262397.3:c.231T=	XP_005262454.1:p.Val77=
XM_005262397.4:c.231T=	XP_005262454.1:p.Val77=
NM_000133.4:c.231T= MANE Select	NP_000124.1:p.Val77=
NM_001313913.2:c.231T=	NP_001300842.1:p.Val77=