Canonical Allele Identifier: CA518861765

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138633315T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551156T>A , CM000685.2:g.139551156T>A	GRCh38
NC_000023.10:g.138633315T>A , CM000685.1:g.138633315T>A	GRCh37
NC_000023.9:g.138460981T>A	NCBI36
NG_007994.1:g.25421T>A , LRG_556:g.25421T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.615T>A MANE Select	ENSP00000218099.2:p.Thr205=
ENST00000643157.1:n.1282T>A
ENST00000218099.6:c.615T>A	ENSP00000218099.2:p.Thr205=
ENST00000394090.2:c.501T>A	ENSP00000377650.2:p.Thr167=
NM_000133.3:c.615T>A , LRG_556t1:c.615T>A	NP_000124.1:p.Thr205=
NM_001313913.1:c.501T>A	NP_001300842.1:p.Thr167=
XM_005262397.3:c.486T>A	XP_005262454.1:p.Thr162=
XM_005262397.4:c.486T>A	XP_005262454.1:p.Thr162=
NM_000133.4:c.615T>A MANE Select	NP_000124.1:p.Thr205=
NM_001313913.2:c.501T>A	NP_001300842.1:p.Thr167=