Canonical Allele Identifier: CA414443521

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138642976A>G (hg19) ; chrX:g.139560817A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560817A>G , CM000685.2:g.139560817A>G	GRCh38
NC_000023.10:g.138642976A>G , CM000685.1:g.138642976A>G	GRCh37
NC_000023.9:g.138470642A>G	NCBI36
NG_007994.1:g.35082A>G , LRG_556:g.35082A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.800A>G MANE Select	ENSP00000218099.2:p.His267Arg
ENST00000643157.1:n.1467A>G
ENST00000218099.6:c.800A>G	ENSP00000218099.2:p.His267Arg
ENST00000394090.2:c.686A>G	ENSP00000377650.2:p.His229Arg
NM_000133.3:c.800A>G , LRG_556t1:c.800A>G	NP_000124.1:p.His267Arg
NM_001313913.1:c.686A>G	NP_001300842.1:p.His229Arg
XM_005262397.3:c.671A>G	XP_005262454.1:p.His224Arg
XM_005262397.4:c.671A>G	XP_005262454.1:p.His224Arg
NM_000133.4:c.800A>G MANE Select	NP_000124.1:p.His267Arg
NM_001313913.2:c.686A>G	NP_001300842.1:p.His229Arg