Canonical Allele Identifier: CA518861646

Gene: F9

Linked Data

• ClinVar Variation Id: 2932533
• ClinVar RCV Id: RCV003795747
• dbSNP Id: rs1603265792
• gnomAD v3: X-139551096-A-G
• gnomAD v4: X-139551096-A-G
• MyVariant Identifiers: chrX:g.138633255A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551096A>G , CM000685.2:g.139551096A>G	GRCh38
NC_000023.10:g.138633255A>G , CM000685.1:g.138633255A>G	GRCh37
NC_000023.9:g.138460921A>G	NCBI36
NG_007994.1:g.25361A>G , LRG_556:g.25361A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.555A>G MANE Select	ENSP00000218099.2:p.Gln185=
ENST00000643157.1:n.1222A>G
ENST00000218099.6:c.555A>G	ENSP00000218099.2:p.Gln185=
ENST00000394090.2:c.441A>G	ENSP00000377650.2:p.Gln147=
NM_000133.3:c.555A>G , LRG_556t1:c.555A>G	NP_000124.1:p.Gln185=
NM_001313913.1:c.441A>G	NP_001300842.1:p.Gln147=
XM_005262397.3:c.426A>G	XP_005262454.1:p.Gln142=
XM_005262397.4:c.426A>G	XP_005262454.1:p.Gln142=
NM_000133.4:c.555A>G MANE Select	NP_000124.1:p.Gln185=
NM_001313913.2:c.441A>G	NP_001300842.1:p.Gln147=