Canonical Allele Identifier: CA414446636

Gene: F9

Linked Data

• ClinVar Variation Id: 994026
• ClinVar RCV Id: RCV001813028
• dbSNP Id: rs1928125452
• MyVariant Identifiers: chrX:g.138644073A>T (hg19) ; chrX:g.139561914A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561914A>T , CM000685.2:g.139561914A>T	GRCh38
NC_000023.10:g.138644073A>T , CM000685.1:g.138644073A>T	GRCh37
NC_000023.9:g.138471739A>T	NCBI36
NG_007994.1:g.36179A>T , LRG_556:g.36179A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1229A>T MANE Select	ENSP00000218099.2:p.Asp410Val
ENST00000643157.1:n.1723+173A>T
ENST00000218099.6:c.1229A>T	ENSP00000218099.2:p.Asp410Val
ENST00000394090.2:c.1115A>T	ENSP00000377650.2:p.Asp372Val
NM_000133.3:c.1229A>T , LRG_556t1:c.1229A>T	NP_000124.1:p.Asp410Val
NM_001313913.1:c.1115A>T	NP_001300842.1:p.Asp372Val
XM_005262397.3:c.1100A>T	XP_005262454.1:p.Asp367Val
XM_005262397.4:c.1100A>T	XP_005262454.1:p.Asp367Val
NM_000133.4:c.1229A>T MANE Select	NP_000124.1:p.Asp410Val
NM_001313913.2:c.1115A>T	NP_001300842.1:p.Asp372Val