Canonical Allele Identifier: CA414444668

Gene: F9

Linked Data

• ClinVar Variation Id: 973817
• ClinVar RCV Id: RCV001265103
• dbSNP Id: rs1371397743
• MyVariant Identifiers: chrX:g.138643731T>A (hg19) ; chrX:g.139561572T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561572T>A , CM000685.2:g.139561572T>A	GRCh38
NC_000023.10:g.138643731T>A , CM000685.1:g.138643731T>A	GRCh37
NC_000023.9:g.138471397T>A	NCBI36
NG_007994.1:g.35837T>A , LRG_556:g.35837T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.887T>A MANE Select	ENSP00000218099.2:p.Val296Glu
ENST00000643157.1:n.1554T>A
ENST00000218099.6:c.887T>A	ENSP00000218099.2:p.Val296Glu
ENST00000394090.2:c.773T>A	ENSP00000377650.2:p.Val258Glu
NM_000133.3:c.887T>A , LRG_556t1:c.887T>A	NP_000124.1:p.Val296Glu
NM_001313913.1:c.773T>A	NP_001300842.1:p.Val258Glu
XM_005262397.3:c.758T>A	XP_005262454.1:p.Val253Glu
XM_005262397.4:c.758T>A	XP_005262454.1:p.Val253Glu
NM_000133.4:c.887T>A MANE Select	NP_000124.1:p.Val296Glu
NM_001313913.2:c.773T>A	NP_001300842.1:p.Val258Glu