Canonical Allele Identifier: CA2461405453

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541046G= , CM000685.2:g.139541046G=	GRCh38
NC_000023.10:g.138623205G= , CM000685.1:g.138623205G=	GRCh37
NC_000023.9:g.138450871G=	NCBI36
NG_007994.1:g.15311G= , LRG_556:g.15311G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.278-30G= MANE Select	ENSP00000218099.2:n.278-30G=
ENST00000218099.6:c.278-30G=	ENSP00000218099.2:n.278-30G=
ENST00000394090.2:c.277+3660G=	ENSP00000377650.2:n.277+3660G=
ENST00000479617.2:n.242-41G=
NM_000133.3:c.278-30G= , LRG_556t1:c.278-30G=	NP_000124.1:n.278-30G=
NM_001313913.1:c.277+3660G=	NP_001300842.1:n.277+3660G=
XM_005262397.3:c.278-30G=	XP_005262454.1:n.278-30G=
XM_005262397.4:c.278-30G=	XP_005262454.1:n.278-30G=
NM_000133.4:c.278-30G= MANE Select	NP_000124.1:n.278-30G=
NM_001313913.2:c.277+3660G=	NP_001300842.1:n.277+3660G=