Canonical Allele Identifier: CA255437

Gene: F9

Linked Data

• ClinVar Variation Id: 10647
• ClinVar RCV Id: RCV000011393 ; RCV001810851
• dbSNP Id: rs137852275
• MyVariant Identifiers: chrX:g.138643914G>A (hg19) ; chrX:g.139561755G>A (hg38)
• PubMed: PMID:1958666

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561755G>A , CM000685.2:g.139561755G>A	GRCh38
NC_000023.10:g.138643914G>A , CM000685.1:g.138643914G>A	GRCh37
NC_000023.9:g.138471580G>A	NCBI36
NG_007994.1:g.36020G>A , LRG_556:g.36020G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1070G>A MANE Select	ENSP00000218099.2:p.Gly357Glu
ENST00000643157.1:n.1723+14G>A
ENST00000218099.6:c.1070G>A	ENSP00000218099.2:p.Gly357Glu
ENST00000394090.2:c.956G>A	ENSP00000377650.2:p.Gly319Glu
NM_000133.3:c.1070G>A , LRG_556t1:c.1070G>A	NP_000124.1:p.Gly357Glu
NM_001313913.1:c.956G>A	NP_001300842.1:p.Gly319Glu
XM_005262397.3:c.941G>A	XP_005262454.1:p.Gly314Glu
XM_005262397.4:c.941G>A	XP_005262454.1:p.Gly314Glu
NM_000133.4:c.1070G>A MANE Select	NP_000124.1:p.Gly357Glu
NM_001313913.2:c.956G>A	NP_001300842.1:p.Gly319Glu