Canonical Allele Identifier: CA2461411837

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560821T= , CM000685.2:g.139560821T=	GRCh38
NC_000023.10:g.138642980T= , CM000685.1:g.138642980T=	GRCh37
NC_000023.9:g.138470646T=	NCBI36
NG_007994.1:g.35086T= , LRG_556:g.35086T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000133.4:c.804T= MANE Select	NP_000124.1:p.Cys268=
ENST00000218099.7:c.804T= MANE Select	ENSP00000218099.2:p.Cys268=
NM_000133.3:c.804T= , LRG_556t1:c.804T=	NP_000124.1:p.Cys268=
NM_001313913.1:c.690T=	NP_001300842.1:p.Cys230=
NM_001313913.2:c.690T=	NP_001300842.1:p.Cys230=
ENST00000218099.6:c.804T=	ENSP00000218099.2:p.Cys268=
ENST00000394090.2:c.690T=	ENSP00000377650.2:p.Cys230=
ENST00000643157.1:n.1471T=
XM_005262397.3:c.675T=	XP_005262454.1:p.Cys225=
XM_005262397.4:c.675T=	XP_005262454.1:p.Cys225=