Canonical Allele Identifier: CA2461408552

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139550940A= , CM000685.2:g.139550940A=	GRCh38
NC_000023.10:g.138633099A= , CM000685.1:g.138633099A=	GRCh37
NC_000023.9:g.138460765A=	NCBI36
NG_007994.1:g.25205A= , LRG_556:g.25205A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.521-122A= MANE Select	ENSP00000218099.2:n.521-122A=
ENST00000643157.1:n.1188-122A=
ENST00000218099.6:c.521-122A=	ENSP00000218099.2:n.521-122A=
ENST00000394090.2:c.407-122A=	ENSP00000377650.2:n.407-122A=
NM_000133.3:c.521-122A= , LRG_556t1:c.521-122A=	NP_000124.1:n.521-122A=
NM_001313913.1:c.407-122A=	NP_001300842.1:n.407-122A=
XM_005262397.3:c.392-122A=	XP_005262454.1:n.392-122A=
XM_005262397.4:c.392-122A=	XP_005262454.1:n.392-122A=
NM_000133.4:c.521-122A= MANE Select	NP_000124.1:n.521-122A=
NM_001313913.2:c.407-122A=	NP_001300842.1:n.407-122A=