Canonical Allele Identifier: CA255344

Gene: F9

Linked Data

• ClinVar Variation Id: 10587
• ClinVar RCV Id: RCV000011333 ; RCV001000167 ; RCV001069256
• dbSNP Id: rs137852248
• MyVariant Identifiers: chrX:g.138643724C>T (hg19) ; chrX:g.139561565C>T (hg38)
• PubMed: PMID:2743975

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561565C>T , CM000685.2:g.139561565C>T	GRCh38
NC_000023.10:g.138643724C>T , CM000685.1:g.138643724C>T	GRCh37
NC_000023.9:g.138471390C>T	NCBI36
NG_007994.1:g.35830C>T , LRG_556:g.35830C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.880C>T MANE Select	ENSP00000218099.2:p.Arg294Ter
ENST00000643157.1:n.1547C>T
ENST00000218099.6:c.880C>T	ENSP00000218099.2:p.Arg294Ter
ENST00000394090.2:c.766C>T	ENSP00000377650.2:p.Arg256Ter
NM_000133.3:c.880C>T , LRG_556t1:c.880C>T	NP_000124.1:p.Arg294Ter
NM_001313913.1:c.766C>T	NP_001300842.1:p.Arg256Ter
XM_005262397.3:c.751C>T	XP_005262454.1:p.Arg251Ter
XM_005262397.4:c.751C>T	XP_005262454.1:p.Arg251Ter
NM_000133.4:c.880C>T MANE Select	NP_000124.1:p.Arg294Ter
NM_001313913.2:c.766C>T	NP_001300842.1:p.Arg256Ter