Canonical Allele Identifier: CA414436208

Gene: F9

Linked Data

• COSMIC: COSM1292940
• MyVariant Identifiers: chrX:g.138619312T>G (hg19) ; chrX:g.139537153T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537153T>G , CM000685.2:g.139537153T>G	GRCh38
NC_000023.10:g.138619312T>G , CM000685.1:g.138619312T>G	GRCh37
NC_000023.9:g.138446978T>G	NCBI36
NG_007994.1:g.11418T>G , LRG_556:g.11418T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.232T>G MANE Select	ENSP00000218099.2:p.Phe78Val
ENST00000218099.6:c.232T>G	ENSP00000218099.2:p.Phe78Val
ENST00000394090.2:c.232T>G	ENSP00000377650.2:p.Phe78Val
ENST00000479617.2:n.239T>G
NM_000133.3:c.232T>G , LRG_556t1:c.232T>G	NP_000124.1:p.Phe78Val
NM_001313913.1:c.232T>G	NP_001300842.1:p.Phe78Val
XM_005262397.3:c.232T>G	XP_005262454.1:p.Phe78Val
XM_005262397.4:c.232T>G	XP_005262454.1:p.Phe78Val
NM_000133.4:c.232T>G MANE Select	NP_000124.1:p.Phe78Val
NM_001313913.2:c.232T>G	NP_001300842.1:p.Phe78Val