Canonical Allele Identifier: CA255416

Gene: F9

Linked Data

• ClinVar Variation Id: 10623
• ClinVar RCV Id: RCV000011369
• dbSNP Id: rs137852266
• MyVariant Identifiers: chrX:g.138644151C>T (hg19) ; chrX:g.139561992C>T (hg38)
• PubMed: PMID:734633 ; PMID:3243764

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561992C>T , CM000685.2:g.139561992C>T	GRCh38
NC_000023.10:g.138644151C>T , CM000685.1:g.138644151C>T	GRCh37
NC_000023.9:g.138471817C>T	NCBI36
NG_007994.1:g.36257C>T , LRG_556:g.36257C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1307C>T MANE Select	ENSP00000218099.2:p.Ala436Val
ENST00000643157.1:n.1723+251C>T
ENST00000218099.6:c.1307C>T	ENSP00000218099.2:p.Ala436Val
ENST00000394090.2:c.1193C>T	ENSP00000377650.2:p.Ala398Val
NM_000133.3:c.1307C>T , LRG_556t1:c.1307C>T	NP_000124.1:p.Ala436Val
NM_001313913.1:c.1193C>T	NP_001300842.1:p.Ala398Val
XM_005262397.3:c.1178C>T	XP_005262454.1:p.Ala393Val
XM_005262397.4:c.1178C>T	XP_005262454.1:p.Ala393Val
NM_000133.4:c.1307C>T MANE Select	NP_000124.1:p.Ala436Val
NM_001313913.2:c.1193C>T	NP_001300842.1:p.Ala398Val