Canonical Allele Identifier: CA414444400

Gene: F9

Linked Data

• ClinVar Variation Id: 1070513
• ClinVar RCV Id: RCV001382694
• dbSNP Id: rs1275842849
• MyVariant Identifiers: chrX:g.138643683G>A (hg19) ; chrX:g.139561524G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561524G>A , CM000685.2:g.139561524G>A	GRCh38
NC_000023.10:g.138643683G>A , CM000685.1:g.138643683G>A	GRCh37
NC_000023.9:g.138471349G>A	NCBI36
NG_007994.1:g.35789G>A , LRG_556:g.35789G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.839G>A MANE Select	ENSP00000218099.2:p.Gly280Asp
ENST00000643157.1:n.1506G>A
ENST00000218099.6:c.839G>A	ENSP00000218099.2:p.Gly280Asp
ENST00000394090.2:c.725G>A	ENSP00000377650.2:p.Gly242Asp
NM_000133.3:c.839G>A , LRG_556t1:c.839G>A	NP_000124.1:p.Gly280Asp
NM_001313913.1:c.725G>A	NP_001300842.1:p.Gly242Asp
XM_005262397.3:c.710G>A	XP_005262454.1:p.Gly237Asp
XM_005262397.4:c.710G>A	XP_005262454.1:p.Gly237Asp
NM_000133.4:c.839G>A MANE Select	NP_000124.1:p.Gly280Asp
NM_001313913.2:c.725G>A	NP_001300842.1:p.Gly242Asp