Canonical Allele Identifier: CA336143170

Gene: F9

Linked Data

• ClinVar Variation Id: 1898807
• ClinVar RCV Id: RCV002574102
• dbSNP Id: rs528270752
• gnomAD v2: X-138643813-A-G
• gnomAD v3: X-139561654-A-G
• gnomAD v4: X-139561654-A-G
• MyVariant Identifiers: chrX:g.138643813A>G (hg19) ; chrX:g.139561654A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561654A>G , CM000685.2:g.139561654A>G	GRCh38
NC_000023.10:g.138643813A>G , CM000685.1:g.138643813A>G	GRCh37
NC_000023.9:g.138471479A>G	NCBI36
NG_007994.1:g.35919A>G , LRG_556:g.35919A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.969A>G MANE Select	ENSP00000218099.2:p.Glu323=
ENST00000643157.1:n.1636A>G
ENST00000218099.6:c.969A>G	ENSP00000218099.2:p.Glu323=
ENST00000394090.2:c.855A>G	ENSP00000377650.2:p.Glu285=
NM_000133.3:c.969A>G , LRG_556t1:c.969A>G	NP_000124.1:p.Glu323=
NM_001313913.1:c.855A>G	NP_001300842.1:p.Glu285=
XM_005262397.3:c.840A>G	XP_005262454.1:p.Glu280=
XM_005262397.4:c.840A>G	XP_005262454.1:p.Glu280=
NM_000133.4:c.969A>G MANE Select	NP_000124.1:p.Glu323=
NM_001313913.2:c.855A>G	NP_001300842.1:p.Glu285=