Canonical Allele Identifier: CA255441

Gene: F9

Linked Data

• ClinVar Variation Id: 10650
• ClinVar RCV Id: RCV000011396 ; RCV002512972
• dbSNP Id: rs137852277
• MyVariant Identifiers: chrX:g.138644075A>G (hg19) ; chrX:g.139561916A>G (hg38)
• PubMed: PMID:1346975

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561916A>G , CM000685.2:g.139561916A>G	GRCh38
NC_000023.10:g.138644075A>G , CM000685.1:g.138644075A>G	GRCh37
NC_000023.9:g.138471741A>G	NCBI36
NG_007994.1:g.36181A>G , LRG_556:g.36181A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1231A>G MANE Select	ENSP00000218099.2:p.Ser411Gly
ENST00000643157.1:n.1723+175A>G
ENST00000218099.6:c.1231A>G	ENSP00000218099.2:p.Ser411Gly
ENST00000394090.2:c.1117A>G	ENSP00000377650.2:p.Ser373Gly
NM_000133.3:c.1231A>G , LRG_556t1:c.1231A>G	NP_000124.1:p.Ser411Gly
NM_001313913.1:c.1117A>G	NP_001300842.1:p.Ser373Gly
XM_005262397.3:c.1102A>G	XP_005262454.1:p.Ser368Gly
XM_005262397.4:c.1102A>G	XP_005262454.1:p.Ser368Gly
NM_000133.4:c.1231A>G MANE Select	NP_000124.1:p.Ser411Gly
NM_001313913.2:c.1117A>G	NP_001300842.1:p.Ser373Gly