Canonical Allele Identifier: CA518861599

Gene: F9

Linked Data

• ClinVar Variation Id: 1078414
• ClinVar RCV Id: RCV001393347
• dbSNP Id: rs2148362379
• MyVariant Identifiers: chrX:g.138633222G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551063G>A , CM000685.2:g.139551063G>A	GRCh38
NC_000023.10:g.138633222G>A , CM000685.1:g.138633222G>A	GRCh37
NC_000023.9:g.138460888G>A	NCBI36
NG_007994.1:g.25328G>A , LRG_556:g.25328G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.522G>A MANE Select	ENSP00000218099.2:p.Val174=
ENST00000643157.1:n.1189G>A
ENST00000218099.6:c.522G>A	ENSP00000218099.2:p.Val174=
ENST00000394090.2:c.408G>A	ENSP00000377650.2:p.Val136=
NM_000133.3:c.522G>A , LRG_556t1:c.522G>A	NP_000124.1:p.Val174=
NM_001313913.1:c.408G>A	NP_001300842.1:p.Val136=
XM_005262397.3:c.393G>A	XP_005262454.1:p.Val131=
XM_005262397.4:c.393G>A	XP_005262454.1:p.Val131=
NM_000133.4:c.522G>A MANE Select	NP_000124.1:p.Val174=
NM_001313913.2:c.408G>A	NP_001300842.1:p.Val136=