Canonical Allele Identifier: CA414440628

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138633287T>A (hg19) ; chrX:g.139551128T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551128T>A , CM000685.2:g.139551128T>A	GRCh38
NC_000023.10:g.138633287T>A , CM000685.1:g.138633287T>A	GRCh37
NC_000023.9:g.138460953T>A	NCBI36
NG_007994.1:g.25393T>A , LRG_556:g.25393T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.587T>A MANE Select	ENSP00000218099.2:p.Phe196Tyr
ENST00000643157.1:n.1254T>A
ENST00000218099.6:c.587T>A	ENSP00000218099.2:p.Phe196Tyr
ENST00000394090.2:c.473T>A	ENSP00000377650.2:p.Phe158Tyr
NM_000133.3:c.587T>A , LRG_556t1:c.587T>A	NP_000124.1:p.Phe196Tyr
NM_001313913.1:c.473T>A	NP_001300842.1:p.Phe158Tyr
XM_005262397.3:c.458T>A	XP_005262454.1:p.Phe153Tyr
XM_005262397.4:c.458T>A	XP_005262454.1:p.Phe153Tyr
NM_000133.4:c.587T>A MANE Select	NP_000124.1:p.Phe196Tyr
NM_001313913.2:c.473T>A	NP_001300842.1:p.Phe158Tyr