Canonical Allele Identifier: CA414445041

Gene: F9

Linked Data

• dbSNP Id: rs150351950
• MyVariant Identifiers: chrX:g.138643811G>T (hg19) ; chrX:g.139561652G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561652G>T , CM000685.2:g.139561652G>T	GRCh38
NC_000023.10:g.138643811G>T , CM000685.1:g.138643811G>T	GRCh37
NC_000023.9:g.138471477G>T	NCBI36
NG_007994.1:g.35917G>T , LRG_556:g.35917G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.967G>T MANE Select	ENSP00000218099.2:p.Glu323Ter
ENST00000643157.1:n.1634G>T
ENST00000218099.6:c.967G>T	ENSP00000218099.2:p.Glu323Ter
ENST00000394090.2:c.853G>T	ENSP00000377650.2:p.Glu285Ter
NM_000133.3:c.967G>T , LRG_556t1:c.967G>T	NP_000124.1:p.Glu323Ter
NM_001313913.1:c.853G>T	NP_001300842.1:p.Glu285Ter
XM_005262397.3:c.838G>T	XP_005262454.1:p.Glu280Ter
XM_005262397.4:c.838G>T	XP_005262454.1:p.Glu280Ter
NM_000133.4:c.967G>T MANE Select	NP_000124.1:p.Glu323Ter
NM_001313913.2:c.853G>T	NP_001300842.1:p.Glu285Ter