Canonical Allele Identifier: CA414444676

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138643733A>G (hg19) ; chrX:g.139561574A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561574A>G , CM000685.2:g.139561574A>G	GRCh38
NC_000023.10:g.138643733A>G , CM000685.1:g.138643733A>G	GRCh37
NC_000023.9:g.138471399A>G	NCBI36
NG_007994.1:g.35839A>G , LRG_556:g.35839A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.889A>G MANE Select	ENSP00000218099.2:p.Ile297Val
ENST00000643157.1:n.1556A>G
ENST00000218099.6:c.889A>G	ENSP00000218099.2:p.Ile297Val
ENST00000394090.2:c.775A>G	ENSP00000377650.2:p.Ile259Val
NM_000133.3:c.889A>G , LRG_556t1:c.889A>G	NP_000124.1:p.Ile297Val
NM_001313913.1:c.775A>G	NP_001300842.1:p.Ile259Val
XM_005262397.3:c.760A>G	XP_005262454.1:p.Ile254Val
XM_005262397.4:c.760A>G	XP_005262454.1:p.Ile254Val
NM_000133.4:c.889A>G MANE Select	NP_000124.1:p.Ile297Val
NM_001313913.2:c.775A>G	NP_001300842.1:p.Ile259Val