Canonical Allele Identifier: CA414435396

Gene: F9

Linked Data

• ClinVar Variation Id: 1078704
• ClinVar RCV Id: RCV001393734
• dbSNP Id: rs1169714103
• gnomAD v2: X-138619186-A-G
• gnomAD v3: X-139537027-A-G
• gnomAD v4: X-139537027-A-G
• MyVariant Identifiers: chrX:g.138619186A>G (hg19) ; chrX:g.139537027A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537027A>G , CM000685.2:g.139537027A>G	GRCh38
NC_000023.10:g.138619186A>G , CM000685.1:g.138619186A>G	GRCh37
NC_000023.9:g.138446852A>G	NCBI36
NG_007994.1:g.11292A>G , LRG_556:g.11292A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.106A>G MANE Select	ENSP00000218099.2:p.Asn36Asp
ENST00000218099.6:c.106A>G	ENSP00000218099.2:p.Asn36Asp
ENST00000394090.2:c.106A>G	ENSP00000377650.2:p.Asn36Asp
ENST00000479617.2:n.113A>G
NM_000133.3:c.106A>G , LRG_556t1:c.106A>G	NP_000124.1:p.Asn36Asp
NM_001313913.1:c.106A>G	NP_001300842.1:p.Asn36Asp
XM_005262397.3:c.106A>G	XP_005262454.1:p.Asn36Asp
XM_005262397.4:c.106A>G	XP_005262454.1:p.Asn36Asp
NM_000133.4:c.106A>G MANE Select	NP_000124.1:p.Asn36Asp
NM_001313913.2:c.106A>G	NP_001300842.1:p.Asn36Asp