Canonical Allele Identifier: CA414446709

Gene: F9

Linked Data

• ClinVar Variation Id: 2775451
• ClinVar RCV Id: RCV003510979
• dbSNP Id: rs1233706534
• MyVariant Identifiers: chrX:g.138644079G>A (hg19) ; chrX:g.139561920G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561920G>A , CM000685.2:g.139561920G>A	GRCh38
NC_000023.10:g.138644079G>A , CM000685.1:g.138644079G>A	GRCh37
NC_000023.9:g.138471745G>A	NCBI36
NG_007994.1:g.36185G>A , LRG_556:g.36185G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1235G>A MANE Select	ENSP00000218099.2:p.Gly412Glu
ENST00000643157.1:n.1723+179G>A
ENST00000218099.6:c.1235G>A	ENSP00000218099.2:p.Gly412Glu
ENST00000394090.2:c.1121G>A	ENSP00000377650.2:p.Gly374Glu
NM_000133.3:c.1235G>A , LRG_556t1:c.1235G>A	NP_000124.1:p.Gly412Glu
NM_001313913.1:c.1121G>A	NP_001300842.1:p.Gly374Glu
XM_005262397.3:c.1106G>A	XP_005262454.1:p.Gly369Glu
XM_005262397.4:c.1106G>A	XP_005262454.1:p.Gly369Glu
NM_000133.4:c.1235G>A MANE Select	NP_000124.1:p.Gly412Glu
NM_001313913.2:c.1121G>A	NP_001300842.1:p.Gly374Glu