Canonical Allele Identifier: CA10529869

Gene: F9

Linked Data

• dbSNP Id: rs113427375
• ExAC: X:138643936 A / G
• gnomAD v2: X-138643936-A-G
• gnomAD v3: X-139561777-A-G
• gnomAD v4: X-139561777-A-G
• MyVariant Identifiers: chrX:g.138643936A>G (hg19) ; chrX:g.139561777A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561777A>G , CM000685.2:g.139561777A>G	GRCh38
NC_000023.10:g.138643936A>G , CM000685.1:g.138643936A>G	GRCh37
NC_000023.9:g.138471602A>G	NCBI36
NG_007994.1:g.36042A>G , LRG_556:g.36042A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1092A>G MANE Select	ENSP00000218099.2:p.Arg364=
ENST00000643157.1:n.1723+36A>G
ENST00000218099.6:c.1092A>G	ENSP00000218099.2:p.Arg364=
ENST00000394090.2:c.978A>G	ENSP00000377650.2:p.Arg326=
NM_000133.3:c.1092A>G , LRG_556t1:c.1092A>G	NP_000124.1:p.Arg364=
NM_001313913.1:c.978A>G	NP_001300842.1:p.Arg326=
XM_005262397.3:c.963A>G	XP_005262454.1:p.Arg321=
XM_005262397.4:c.963A>G	XP_005262454.1:p.Arg321=
NM_000133.4:c.1092A>G MANE Select	NP_000124.1:p.Arg364=
NM_001313913.2:c.978A>G	NP_001300842.1:p.Arg326=