Canonical Allele Identifier: CA414447122

Gene: F9

Linked Data

• ClinVar Variation Id: 812043
• ClinVar RCV Id: RCV001002616
• dbSNP Id: rs762229532
• MyVariant Identifiers: chrX:g.138644134C>A (hg19) ; chrX:g.139561975C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561975C>A , CM000685.2:g.139561975C>A	GRCh38
NC_000023.10:g.138644134C>A , CM000685.1:g.138644134C>A	GRCh37
NC_000023.9:g.138471800C>A	NCBI36
NG_007994.1:g.36240C>A , LRG_556:g.36240C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1290C>A MANE Select	ENSP00000218099.2:p.Ser430Arg
ENST00000643157.1:n.1723+234C>A
ENST00000218099.6:c.1290C>A	ENSP00000218099.2:p.Ser430Arg
ENST00000394090.2:c.1176C>A	ENSP00000377650.2:p.Ser392Arg
NM_000133.3:c.1290C>A , LRG_556t1:c.1290C>A	NP_000124.1:p.Ser430Arg
NM_001313913.1:c.1176C>A	NP_001300842.1:p.Ser392Arg
XM_005262397.3:c.1161C>A	XP_005262454.1:p.Ser387Arg
XM_005262397.4:c.1161C>A	XP_005262454.1:p.Ser387Arg
NM_000133.4:c.1290C>A MANE Select	NP_000124.1:p.Ser430Arg
NM_001313913.2:c.1176C>A	NP_001300842.1:p.Ser392Arg