Canonical Allele Identifier: CA10587386

Gene: F9

Linked Data

• ClinVar Variation Id: 255226
• ClinVar RCV Id: RCV000254250
• dbSNP Id: rs886038243
• COSMIC: COSM1163554
• MyVariant Identifiers: chrX:g.138643876C>T (hg19) ; chrX:g.139561717C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561717C>T , CM000685.2:g.139561717C>T	GRCh38
NC_000023.10:g.138643876C>T , CM000685.1:g.138643876C>T	GRCh37
NC_000023.9:g.138471542C>T	NCBI36
NG_007994.1:g.35982C>T , LRG_556:g.35982C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1032C>T MANE Select	ENSP00000218099.2:p.Ile344=
ENST00000643157.1:n.1699C>T
ENST00000218099.6:c.1032C>T	ENSP00000218099.2:p.Ile344=
ENST00000394090.2:c.918C>T	ENSP00000377650.2:p.Ile306=
NM_000133.3:c.1032C>T , LRG_556t1:c.1032C>T	NP_000124.1:p.Ile344=
NM_001313913.1:c.918C>T	NP_001300842.1:p.Ile306=
XM_005262397.3:c.903C>T	XP_005262454.1:p.Ile301=
XM_005262397.4:c.903C>T	XP_005262454.1:p.Ile301=
NM_000133.4:c.1032C>T MANE Select	NP_000124.1:p.Ile344=
NM_001313913.2:c.918C>T	NP_001300842.1:p.Ile306=