Canonical Allele Identifier: CA518861630

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138633243T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551084T>G , CM000685.2:g.139551084T>G	GRCh38
NC_000023.10:g.138633243T>G , CM000685.1:g.138633243T>G	GRCh37
NC_000023.9:g.138460909T>G	NCBI36
NG_007994.1:g.25349T>G , LRG_556:g.25349T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.543T>G MANE Select	ENSP00000218099.2:p.Val181=
ENST00000643157.1:n.1210T>G
ENST00000218099.6:c.543T>G	ENSP00000218099.2:p.Val181=
ENST00000394090.2:c.429T>G	ENSP00000377650.2:p.Val143=
NM_000133.3:c.543T>G , LRG_556t1:c.543T>G	NP_000124.1:p.Val181=
NM_001313913.1:c.429T>G	NP_001300842.1:p.Val143=
XM_005262397.3:c.414T>G	XP_005262454.1:p.Val138=
XM_005262397.4:c.414T>G	XP_005262454.1:p.Val138=
NM_000133.4:c.543T>G MANE Select	NP_000124.1:p.Val181=
NM_001313913.2:c.429T>G	NP_001300842.1:p.Val143=