Canonical Allele Identifier: CA518864005

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138644107G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561948G>T , CM000685.2:g.139561948G>T	GRCh38
NC_000023.10:g.138644107G>T , CM000685.1:g.138644107G>T	GRCh37
NC_000023.9:g.138471773G>T	NCBI36
NG_007994.1:g.36213G>T , LRG_556:g.36213G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1263G>T MANE Select	ENSP00000218099.2:p.Gly421=
ENST00000643157.1:n.1723+207G>T
ENST00000218099.6:c.1263G>T	ENSP00000218099.2:p.Gly421=
ENST00000394090.2:c.1149G>T	ENSP00000377650.2:p.Gly383=
NM_000133.3:c.1263G>T , LRG_556t1:c.1263G>T	NP_000124.1:p.Gly421=
NM_001313913.1:c.1149G>T	NP_001300842.1:p.Gly383=
XM_005262397.3:c.1134G>T	XP_005262454.1:p.Gly378=
XM_005262397.4:c.1134G>T	XP_005262454.1:p.Gly378=
NM_000133.4:c.1263G>T MANE Select	NP_000124.1:p.Gly421=
NM_001313913.2:c.1149G>T	NP_001300842.1:p.Gly383=