Canonical Allele Identifier: CA414439402

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138630636C>A (hg19) ; chrX:g.139548477C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548477C>A , CM000685.2:g.139548477C>A	GRCh38
NC_000023.10:g.138630636C>A , CM000685.1:g.138630636C>A	GRCh37
NC_000023.9:g.138458302C>A	NCBI36
NG_007994.1:g.22742C>A , LRG_556:g.22742C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.506C>A MANE Select	ENSP00000218099.2:p.Ser169Tyr
ENST00000643157.1:n.1173C>A
ENST00000218099.6:c.506C>A	ENSP00000218099.2:p.Ser169Tyr
ENST00000394090.2:c.392C>A	ENSP00000377650.2:p.Ser131Tyr
NM_000133.3:c.506C>A , LRG_556t1:c.506C>A	NP_000124.1:p.Ser169Tyr
NM_001313913.1:c.392C>A	NP_001300842.1:p.Ser131Tyr
XM_005262397.3:c.392-2585C>A	XP_005262454.1:n.392-2585C>A
XM_005262397.4:c.392-2585C>A	XP_005262454.1:n.392-2585C>A
NM_000133.4:c.506C>A MANE Select	NP_000124.1:p.Ser169Tyr
NM_001313913.2:c.392C>A	NP_001300842.1:p.Ser131Tyr