Canonical Allele Identifier: CA518864021

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138644110C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561951C>G , CM000685.2:g.139561951C>G	GRCh38
NC_000023.10:g.138644110C>G , CM000685.1:g.138644110C>G	GRCh37
NC_000023.9:g.138471776C>G	NCBI36
NG_007994.1:g.36216C>G , LRG_556:g.36216C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1266C>G MANE Select	ENSP00000218099.2:p.Thr422=
ENST00000643157.1:n.1723+210C>G
ENST00000218099.6:c.1266C>G	ENSP00000218099.2:p.Thr422=
ENST00000394090.2:c.1152C>G	ENSP00000377650.2:p.Thr384=
NM_000133.3:c.1266C>G , LRG_556t1:c.1266C>G	NP_000124.1:p.Thr422=
NM_001313913.1:c.1152C>G	NP_001300842.1:p.Thr384=
XM_005262397.3:c.1137C>G	XP_005262454.1:p.Thr379=
XM_005262397.4:c.1137C>G	XP_005262454.1:p.Thr379=
NM_000133.4:c.1266C>G MANE Select	NP_000124.1:p.Thr422=
NM_001313913.2:c.1152C>G	NP_001300842.1:p.Thr384=