Canonical Allele Identifier: CA2461408547

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139550929T= , CM000685.2:g.139550929T=	GRCh38
NC_000023.10:g.138633088T= , CM000685.1:g.138633088T=	GRCh37
NC_000023.9:g.138460754T=	NCBI36
NG_007994.1:g.25194T= , LRG_556:g.25194T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.521-133T= MANE Select	ENSP00000218099.2:n.521-133T=
ENST00000643157.1:n.1188-133T=
ENST00000218099.6:c.521-133T=	ENSP00000218099.2:n.521-133T=
ENST00000394090.2:c.407-133T=	ENSP00000377650.2:n.407-133T=
NM_000133.3:c.521-133T= , LRG_556t1:c.521-133T=	NP_000124.1:n.521-133T=
NM_001313913.1:c.407-133T=	NP_001300842.1:n.407-133T=
XM_005262397.3:c.392-133T=	XP_005262454.1:n.392-133T=
XM_005262397.4:c.392-133T=	XP_005262454.1:n.392-133T=
NM_000133.4:c.521-133T= MANE Select	NP_000124.1:n.521-133T=
NM_001313913.2:c.407-133T=	NP_001300842.1:n.407-133T=