Canonical Allele Identifier: CA414444845

Gene: F9

Linked Data

• ClinVar Variation Id: 618645
• ClinVar RCV Id: RCV000757262
• dbSNP Id: rs1569332828
• MyVariant Identifiers: chrX:g.138643778T>G (hg19) ; chrX:g.139561619T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561619T>G , CM000685.2:g.139561619T>G	GRCh38
NC_000023.10:g.138643778T>G , CM000685.1:g.138643778T>G	GRCh37
NC_000023.9:g.138471444T>G	NCBI36
NG_007994.1:g.35884T>G , LRG_556:g.35884T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.934T>G MANE Select	ENSP00000218099.2:p.Tyr312Asp
ENST00000643157.1:n.1601T>G
ENST00000218099.6:c.934T>G	ENSP00000218099.2:p.Tyr312Asp
ENST00000394090.2:c.820T>G	ENSP00000377650.2:p.Tyr274Asp
NM_000133.3:c.934T>G , LRG_556t1:c.934T>G	NP_000124.1:p.Tyr312Asp
NM_001313913.1:c.820T>G	NP_001300842.1:p.Tyr274Asp
XM_005262397.3:c.805T>G	XP_005262454.1:p.Tyr269Asp
XM_005262397.4:c.805T>G	XP_005262454.1:p.Tyr269Asp
NM_000133.4:c.934T>G MANE Select	NP_000124.1:p.Tyr312Asp
NM_001313913.2:c.820T>G	NP_001300842.1:p.Tyr274Asp