Canonical Allele Identifier: CA336137439

Gene: F9

Linked Data

• dbSNP Id: rs866507797
• COSMIC: COSM3558418
• MyVariant Identifiers: chrX:g.138633334G>A (hg19) ; chrX:g.139551175G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551175G>A , CM000685.2:g.139551175G>A	GRCh38
NC_000023.10:g.138633334G>A , CM000685.1:g.138633334G>A	GRCh37
NC_000023.9:g.138461000G>A	NCBI36
NG_007994.1:g.25440G>A , LRG_556:g.25440G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.634G>A MANE Select	ENSP00000218099.2:p.Asp212Asn
ENST00000643157.1:n.1301G>A
ENST00000218099.6:c.634G>A	ENSP00000218099.2:p.Asp212Asn
ENST00000394090.2:c.520G>A	ENSP00000377650.2:p.Asp174Asn
NM_000133.3:c.634G>A , LRG_556t1:c.634G>A	NP_000124.1:p.Asp212Asn
NM_001313913.1:c.520G>A	NP_001300842.1:p.Asp174Asn
XM_005262397.3:c.505G>A	XP_005262454.1:p.Asp169Asn
XM_005262397.4:c.505G>A	XP_005262454.1:p.Asp169Asn
NM_000133.4:c.634G>A MANE Select	NP_000124.1:p.Asp212Asn
NM_001313913.2:c.520G>A	NP_001300842.1:p.Asp174Asn