Canonical Allele Identifier: CA518862115

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138633372C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551213C>T , CM000685.2:g.139551213C>T	GRCh38
NC_000023.10:g.138633372C>T , CM000685.1:g.138633372C>T	GRCh37
NC_000023.9:g.138461038C>T	NCBI36
NG_007994.1:g.25478C>T , LRG_556:g.25478C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.672C>T MANE Select	ENSP00000218099.2:p.Phe224=
ENST00000643157.1:n.1339C>T
ENST00000218099.6:c.672C>T	ENSP00000218099.2:p.Phe224=
ENST00000394090.2:c.558C>T	ENSP00000377650.2:p.Phe186=
NM_000133.3:c.672C>T , LRG_556t1:c.672C>T	NP_000124.1:p.Phe224=
NM_001313913.1:c.558C>T	NP_001300842.1:p.Phe186=
XM_005262397.3:c.543C>T	XP_005262454.1:p.Phe181=
XM_005262397.4:c.543C>T	XP_005262454.1:p.Phe181=
NM_000133.4:c.672C>T MANE Select	NP_000124.1:p.Phe224=
NM_001313913.2:c.558C>T	NP_001300842.1:p.Phe186=