Canonical Allele Identifier: CA414437821

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138623324T>A (hg19) ; chrX:g.139541165T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541165T>A , CM000685.2:g.139541165T>A	GRCh38
NC_000023.10:g.138623324T>A , CM000685.1:g.138623324T>A	GRCh37
NC_000023.9:g.138450990T>A	NCBI36
NG_007994.1:g.15430T>A , LRG_556:g.15430T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.367T>A MANE Select	ENSP00000218099.2:p.Phe123Ile
ENST00000218099.6:c.367T>A	ENSP00000218099.2:p.Phe123Ile
ENST00000394090.2:c.277+3779T>A	ENSP00000377650.2:n.277+3779T>A
ENST00000479617.2:n.320T>A
NM_000133.3:c.367T>A , LRG_556t1:c.367T>A	NP_000124.1:p.Phe123Ile
NM_001313913.1:c.277+3779T>A	NP_001300842.1:n.277+3779T>A
XM_005262397.3:c.367T>A	XP_005262454.1:p.Phe123Ile
XM_005262397.4:c.367T>A	XP_005262454.1:p.Phe123Ile
NM_000133.4:c.367T>A MANE Select	NP_000124.1:p.Phe123Ile
NM_001313913.2:c.277+3779T>A	NP_001300842.1:n.277+3779T>A