Canonical Allele Identifier: CA414443105

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138642915A>G (hg19) ; chrX:g.139560756A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560756A>G , CM000685.2:g.139560756A>G	GRCh38
NC_000023.10:g.138642915A>G , CM000685.1:g.138642915A>G	GRCh37
NC_000023.9:g.138470581A>G	NCBI36
NG_007994.1:g.35021A>G , LRG_556:g.35021A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.739A>G MANE Select	ENSP00000218099.2:p.Lys247Glu
ENST00000643157.1:n.1406A>G
ENST00000218099.6:c.739A>G	ENSP00000218099.2:p.Lys247Glu
ENST00000394090.2:c.625A>G	ENSP00000377650.2:p.Lys209Glu
NM_000133.3:c.739A>G , LRG_556t1:c.739A>G	NP_000124.1:p.Lys247Glu
NM_001313913.1:c.625A>G	NP_001300842.1:p.Lys209Glu
XM_005262397.3:c.610A>G	XP_005262454.1:p.Lys204Glu
XM_005262397.4:c.610A>G	XP_005262454.1:p.Lys204Glu
NM_000133.4:c.739A>G MANE Select	NP_000124.1:p.Lys247Glu
NM_001313913.2:c.625A>G	NP_001300842.1:p.Lys209Glu