Canonical Allele Identifier: CA518861754

Gene: F9

Linked Data

• dbSNP Id: rs1199474371
• gnomAD v2: X-138633312-T-G
• gnomAD v3: X-139551153-T-G
• gnomAD v4: X-139551153-T-G
• MyVariant Identifiers: chrX:g.138633312T>G (hg19) ; chrX:g.139551153T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551153T>G , CM000685.2:g.139551153T>G	GRCh38
NC_000023.10:g.138633312T>G , CM000685.1:g.138633312T>G	GRCh37
NC_000023.9:g.138460978T>G	NCBI36
NG_007994.1:g.25418T>G , LRG_556:g.25418T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.612T>G MANE Select	ENSP00000218099.2:p.Ser204=
ENST00000643157.1:n.1279T>G
ENST00000218099.6:c.612T>G	ENSP00000218099.2:p.Ser204=
ENST00000394090.2:c.498T>G	ENSP00000377650.2:p.Ser166=
NM_000133.3:c.612T>G , LRG_556t1:c.612T>G	NP_000124.1:p.Ser204=
NM_001313913.1:c.498T>G	NP_001300842.1:p.Ser166=
XM_005262397.3:c.483T>G	XP_005262454.1:p.Ser161=
XM_005262397.4:c.483T>G	XP_005262454.1:p.Ser161=
NM_000133.4:c.612T>G MANE Select	NP_000124.1:p.Ser204=
NM_001313913.2:c.498T>G	NP_001300842.1:p.Ser166=