Canonical Allele Identifier: CA414437787

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138623316C>T (hg19) ; chrX:g.139541157C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541157C>T , CM000685.2:g.139541157C>T	GRCh38
NC_000023.10:g.138623316C>T , CM000685.1:g.138623316C>T	GRCh37
NC_000023.9:g.138450982C>T	NCBI36
NG_007994.1:g.15422C>T , LRG_556:g.15422C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.359C>T MANE Select	ENSP00000218099.2:p.Pro120Leu
ENST00000218099.6:c.359C>T	ENSP00000218099.2:p.Pro120Leu
ENST00000394090.2:c.277+3771C>T	ENSP00000377650.2:n.277+3771C>T
ENST00000479617.2:n.312C>T
NM_000133.3:c.359C>T , LRG_556t1:c.359C>T	NP_000124.1:p.Pro120Leu
NM_001313913.1:c.277+3771C>T	NP_001300842.1:n.277+3771C>T
XM_005262397.3:c.359C>T	XP_005262454.1:p.Pro120Leu
XM_005262397.4:c.359C>T	XP_005262454.1:p.Pro120Leu
NM_000133.4:c.359C>T MANE Select	NP_000124.1:p.Pro120Leu
NM_001313913.2:c.277+3771C>T	NP_001300842.1:n.277+3771C>T