Canonical Allele Identifier: CA255373

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561602A>G , CM000685.2:g.139561602A>G	GRCh38
NC_000023.10:g.138643761A>G , CM000685.1:g.138643761A>G	GRCh37
NC_000023.9:g.138471427A>G	NCBI36
NG_007994.1:g.35867A>G , LRG_556:g.35867A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.917A>G MANE Select	ENSP00000218099.2:p.Asn306Ser
ENST00000643157.1:n.1584A>G
ENST00000218099.6:c.917A>G	ENSP00000218099.2:p.Asn306Ser
ENST00000394090.2:c.803A>G	ENSP00000377650.2:p.Asn268Ser
NM_000133.3:c.917A>G , LRG_556t1:c.917A>G	NP_000124.1:p.Asn306Ser
NM_001313913.1:c.803A>G	NP_001300842.1:p.Asn268Ser
XM_005262397.3:c.788A>G	XP_005262454.1:p.Asn263Ser
XM_005262397.4:c.788A>G	XP_005262454.1:p.Asn263Ser
NM_000133.4:c.917A>G MANE Select	NP_000124.1:p.Asn306Ser
NM_001313913.2:c.803A>G	NP_001300842.1:p.Asn268Ser