Canonical Allele Identifier: CA518864311

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138644170A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562011A>G , CM000685.2:g.139562011A>G	GRCh38
NC_000023.10:g.138644170A>G , CM000685.1:g.138644170A>G	GRCh37
NC_000023.9:g.138471836A>G	NCBI36
NG_007994.1:g.36276A>G , LRG_556:g.36276A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1326A>G MANE Select	ENSP00000218099.2:p.Gly442=
ENST00000643157.1:n.1723+270A>G
ENST00000218099.6:c.1326A>G	ENSP00000218099.2:p.Gly442=
ENST00000394090.2:c.1212A>G	ENSP00000377650.2:p.Gly404=
NM_000133.3:c.1326A>G , LRG_556t1:c.1326A>G	NP_000124.1:p.Gly442=
NM_001313913.1:c.1212A>G	NP_001300842.1:p.Gly404=
XM_005262397.3:c.1197A>G	XP_005262454.1:p.Gly399=
XM_005262397.4:c.1197A>G	XP_005262454.1:p.Gly399=
NM_000133.4:c.1326A>G MANE Select	NP_000124.1:p.Gly442=
NM_001313913.2:c.1212A>G	NP_001300842.1:p.Gly404=