Canonical Allele Identifier: CA10529812

Gene: F9

Linked Data

• ClinVar Variation Id: 913851
• ClinVar RCV Id: RCV001514299
• dbSNP Id: rs754155651
• ExAC: X:138633282 T / G
• gnomAD v2: X-138633282-T-G
• gnomAD v3: X-139551123-T-G
• gnomAD v4: X-139551123-T-G
• MyVariant Identifiers: chrX:g.138633282T>G (hg19) ; chrX:g.139551123T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551123T>G , CM000685.2:g.139551123T>G	GRCh38
NC_000023.10:g.138633282T>G , CM000685.1:g.138633282T>G	GRCh37
NC_000023.9:g.138460948T>G	NCBI36
NG_007994.1:g.25388T>G , LRG_556:g.25388T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.582T>G MANE Select	ENSP00000218099.2:p.Thr194=
ENST00000643157.1:n.1249T>G
ENST00000218099.6:c.582T>G	ENSP00000218099.2:p.Thr194=
ENST00000394090.2:c.468T>G	ENSP00000377650.2:p.Thr156=
NM_000133.3:c.582T>G , LRG_556t1:c.582T>G	NP_000124.1:p.Thr194=
NM_001313913.1:c.468T>G	NP_001300842.1:p.Thr156=
XM_005262397.3:c.453T>G	XP_005262454.1:p.Thr151=
XM_005262397.4:c.453T>G	XP_005262454.1:p.Thr151=
NM_000133.4:c.582T>G MANE Select	NP_000124.1:p.Thr194=
NM_001313913.2:c.468T>G	NP_001300842.1:p.Thr156=