Canonical Allele Identifier: CA10529811

Gene: F9

Linked Data

• dbSNP Id: rs756270566
• ExAC: X:138633277 G / A
• gnomAD v2: X-138633277-G-A
• gnomAD v4: X-139551118-G-A
• MyVariant Identifiers: chrX:g.138633277G>A (hg19) ; chrX:g.139551118G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551118G>A , CM000685.2:g.139551118G>A	GRCh38
NC_000023.10:g.138633277G>A , CM000685.1:g.138633277G>A	GRCh37
NC_000023.9:g.138460943G>A	NCBI36
NG_007994.1:g.25383G>A , LRG_556:g.25383G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.577G>A MANE Select	ENSP00000218099.2:p.Glu193Lys
ENST00000643157.1:n.1244G>A
ENST00000218099.6:c.577G>A	ENSP00000218099.2:p.Glu193Lys
ENST00000394090.2:c.463G>A	ENSP00000377650.2:p.Glu155Lys
NM_000133.3:c.577G>A , LRG_556t1:c.577G>A	NP_000124.1:p.Glu193Lys
NM_001313913.1:c.463G>A	NP_001300842.1:p.Glu155Lys
XM_005262397.3:c.448G>A	XP_005262454.1:p.Glu150Lys
XM_005262397.4:c.448G>A	XP_005262454.1:p.Glu150Lys
NM_000133.4:c.577G>A MANE Select	NP_000124.1:p.Glu193Lys
NM_001313913.2:c.463G>A	NP_001300842.1:p.Glu155Lys