Canonical Allele Identifier: CA518917038

Gene: F9

Linked Data

• dbSNP Id: rs1333808596
• gnomAD v2: X-138643927-C-T
• gnomAD v4: X-139561768-C-T
• MyVariant Identifiers: chrX:g.138643927C>T (hg19) ; chrX:g.139561768C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561768C>T , CM000685.2:g.139561768C>T	GRCh38
NC_000023.10:g.138643927C>T , CM000685.1:g.138643927C>T	GRCh37
NC_000023.9:g.138471593C>T	NCBI36
NG_007994.1:g.36033C>T , LRG_556:g.36033C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1083C>T MANE Select	ENSP00000218099.2:p.His361=
ENST00000643157.1:n.1723+27C>T
ENST00000218099.6:c.1083C>T	ENSP00000218099.2:p.His361=
ENST00000394090.2:c.969C>T	ENSP00000377650.2:p.His323=
NM_000133.3:c.1083C>T , LRG_556t1:c.1083C>T	NP_000124.1:p.His361=
NM_001313913.1:c.969C>T	NP_001300842.1:p.His323=
XM_005262397.3:c.954C>T	XP_005262454.1:p.His318=
XM_005262397.4:c.954C>T	XP_005262454.1:p.His318=
NM_000133.4:c.1083C>T MANE Select	NP_000124.1:p.His361=
NM_001313913.2:c.969C>T	NP_001300842.1:p.His323=