Canonical Allele Identifier: CA518916299
Gene: F9 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.138643699G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561540G>A , CM000685.2:g.139561540G>A GRCh38
NC_000023.10:g.138643699G>A , CM000685.1:g.138643699G>A GRCh37
NC_000023.9:g.138471365G>A NCBI36
NG_007994.1:g.35805G>A , LRG_556:g.35805G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.855G>A MANE Select ENSP00000218099.2:p.Glu285=
ENST00000643157.1:n.1522G>A
ENST00000218099.6:c.855G>A ENSP00000218099.2:p.Glu285=
ENST00000394090.2:c.741G>A ENSP00000377650.2:p.Glu247=
NM_000133.3:c.855G>A , LRG_556t1:c.855G>A NP_000124.1:p.Glu285=
NM_001313913.1:c.741G>A NP_001300842.1:p.Glu247=
XM_005262397.3:c.726G>A XP_005262454.1:p.Glu242=
XM_005262397.4:c.726G>A XP_005262454.1:p.Glu242=
NM_000133.4:c.855G>A MANE Select NP_000124.1:p.Glu285=
NM_001313913.2:c.741G>A NP_001300842.1:p.Glu247=