Canonical Allele Identifier: CA2461412321

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562081G= , CM000685.2:g.139562081G=	GRCh38
NC_000023.10:g.138644240G= , CM000685.1:g.138644240G=	GRCh37
NC_000023.9:g.138471906G=	NCBI36
NG_007994.1:g.36346G= , LRG_556:g.36346G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.*10G= MANE Select	ENSP00000218099.2:n.*10G=
ENST00000643157.1:n.1723+340G=
ENST00000218099.6:c.*10G=	ENSP00000218099.2:n.*10G=
NM_000133.3:c.*10G= , LRG_556t1:c.*10G=	NP_000124.1:n.*10G=
NM_001313913.1:c.*10G=	NP_001300842.1:n.*10G=
XM_005262397.3:c.*10G=	XP_005262454.1:n.*10G=
XM_005262397.4:c.*10G=	XP_005262454.1:n.*10G=
NM_000133.4:c.*10G= MANE Select	NP_000124.1:n.*10G=
NM_001313913.2:c.*10G=	NP_001300842.1:n.*10G=