Canonical Allele Identifier: CA336143030

Gene: F9

Linked Data

• ClinVar Variation Id: 627146
• ClinVar RCV Id: RCV000851898
• dbSNP Id: rs753654616
• gnomAD v4: X-139561530-A-G
• MyVariant Identifiers: chrX:g.138643689A>G (hg19) ; chrX:g.139561530A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561530A>G , CM000685.2:g.139561530A>G	GRCh38
NC_000023.10:g.138643689A>G , CM000685.1:g.138643689A>G	GRCh37
NC_000023.9:g.138471355A>G	NCBI36
NG_007994.1:g.35795A>G , LRG_556:g.35795A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.845A>G MANE Select	ENSP00000218099.2:p.His282Arg
ENST00000643157.1:n.1512A>G
ENST00000218099.6:c.845A>G	ENSP00000218099.2:p.His282Arg
ENST00000394090.2:c.731A>G	ENSP00000377650.2:p.His244Arg
NM_000133.3:c.845A>G , LRG_556t1:c.845A>G	NP_000124.1:p.His282Arg
NM_001313913.1:c.731A>G	NP_001300842.1:p.His244Arg
XM_005262397.3:c.716A>G	XP_005262454.1:p.His239Arg
XM_005262397.4:c.716A>G	XP_005262454.1:p.His239Arg
NM_000133.4:c.845A>G MANE Select	NP_000124.1:p.His282Arg
NM_001313913.2:c.731A>G	NP_001300842.1:p.His244Arg