Canonical Allele Identifier: CA414444573

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138643712A>T (hg19) ; chrX:g.139561553A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561553A>T , CM000685.2:g.139561553A>T	GRCh38
NC_000023.10:g.138643712A>T , CM000685.1:g.138643712A>T	GRCh37
NC_000023.9:g.138471378A>T	NCBI36
NG_007994.1:g.35818A>T , LRG_556:g.35818A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.868A>T MANE Select	ENSP00000218099.2:p.Thr290Ser
ENST00000643157.1:n.1535A>T
ENST00000218099.6:c.868A>T	ENSP00000218099.2:p.Thr290Ser
ENST00000394090.2:c.754A>T	ENSP00000377650.2:p.Thr252Ser
NM_000133.3:c.868A>T , LRG_556t1:c.868A>T	NP_000124.1:p.Thr290Ser
NM_001313913.1:c.754A>T	NP_001300842.1:p.Thr252Ser
XM_005262397.3:c.739A>T	XP_005262454.1:p.Thr247Ser
XM_005262397.4:c.739A>T	XP_005262454.1:p.Thr247Ser
NM_000133.4:c.868A>T MANE Select	NP_000124.1:p.Thr290Ser
NM_001313913.2:c.754A>T	NP_001300842.1:p.Thr252Ser