Canonical Allele Identifier: CA336137401

Gene: F9

Linked Data

• dbSNP Id: rs137852237
• COSMIC: COSM3372093
• MyVariant Identifiers: chrX:g.138633271C>A (hg19) ; chrX:g.139551112C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551112C>A , CM000685.2:g.139551112C>A	GRCh38
NC_000023.10:g.138633271C>A , CM000685.1:g.138633271C>A	GRCh37
NC_000023.9:g.138460937C>A	NCBI36
NG_007994.1:g.25377C>A , LRG_556:g.25377C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.571C>A MANE Select	ENSP00000218099.2:p.Arg191Ser
ENST00000643157.1:n.1238C>A
ENST00000218099.6:c.571C>A	ENSP00000218099.2:p.Arg191Ser
ENST00000394090.2:c.457C>A	ENSP00000377650.2:p.Arg153Ser
NM_000133.3:c.571C>A , LRG_556t1:c.571C>A	NP_000124.1:p.Arg191Ser
NM_001313913.1:c.457C>A	NP_001300842.1:p.Arg153Ser
XM_005262397.3:c.442C>A	XP_005262454.1:p.Arg148Ser
XM_005262397.4:c.442C>A	XP_005262454.1:p.Arg148Ser
NM_000133.4:c.571C>A MANE Select	NP_000124.1:p.Arg191Ser
NM_001313913.2:c.457C>A	NP_001300842.1:p.Arg153Ser