Canonical Allele Identifier: CA2461412092

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561592C= , CM000685.2:g.139561592C=	GRCh38
NC_000023.10:g.138643751C= , CM000685.1:g.138643751C=	GRCh37
NC_000023.9:g.138471417C=	NCBI36
NG_007994.1:g.35857C= , LRG_556:g.35857C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000133.4:c.907C= MANE Select	NP_000124.1:p.His303=
ENST00000218099.7:c.907C= MANE Select	ENSP00000218099.2:p.His303=
NM_000133.3:c.907C= , LRG_556t1:c.907C=	NP_000124.1:p.His303=
NM_001313913.1:c.793C=	NP_001300842.1:p.His265=
NM_001313913.2:c.793C=	NP_001300842.1:p.His265=
ENST00000218099.6:c.907C=	ENSP00000218099.2:p.His303=
ENST00000394090.2:c.793C=	ENSP00000377650.2:p.His265=
ENST00000643157.1:n.1574C=
XM_005262397.3:c.778C=	XP_005262454.1:p.His260=
XM_005262397.4:c.778C=	XP_005262454.1:p.His260=