Canonical Allele Identifier: CA414444869

Gene: F9

Linked Data

• gnomAD v4: X-139561626-A-G
• MyVariant Identifiers: chrX:g.138643785A>G (hg19) ; chrX:g.139561626A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561626A>G , CM000685.2:g.139561626A>G	GRCh38
NC_000023.10:g.138643785A>G , CM000685.1:g.138643785A>G	GRCh37
NC_000023.9:g.138471451A>G	NCBI36
NG_007994.1:g.35891A>G , LRG_556:g.35891A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.941A>G MANE Select	ENSP00000218099.2:p.His314Arg
ENST00000643157.1:n.1608A>G
ENST00000218099.6:c.941A>G	ENSP00000218099.2:p.His314Arg
ENST00000394090.2:c.827A>G	ENSP00000377650.2:p.His276Arg
NM_000133.3:c.941A>G , LRG_556t1:c.941A>G	NP_000124.1:p.His314Arg
NM_001313913.1:c.827A>G	NP_001300842.1:p.His276Arg
XM_005262397.3:c.812A>G	XP_005262454.1:p.His271Arg
XM_005262397.4:c.812A>G	XP_005262454.1:p.His271Arg
NM_000133.4:c.941A>G MANE Select	NP_000124.1:p.His314Arg
NM_001313913.2:c.827A>G	NP_001300842.1:p.His276Arg