Canonical Allele Identifier: CA2461408636
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551220G= , CM000685.2:g.139551220G= GRCh38
NC_000023.10:g.138633379G= , CM000685.1:g.138633379G= GRCh37
NC_000023.9:g.138461045G= NCBI36
NG_007994.1:g.25485G= , LRG_556:g.25485G=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.679G= MANE Select ENSP00000218099.2:p.Val227=
ENST00000643157.1:n.1346G=
ENST00000218099.6:c.679G= ENSP00000218099.2:p.Val227=
ENST00000394090.2:c.565G= ENSP00000377650.2:p.Val189=
NM_000133.3:c.679G= , LRG_556t1:c.679G= NP_000124.1:p.Val227=
NM_001313913.1:c.565G= NP_001300842.1:p.Val189=
XM_005262397.3:c.550G= XP_005262454.1:p.Val184=
XM_005262397.4:c.550G= XP_005262454.1:p.Val184=
NM_000133.4:c.679G= MANE Select NP_000124.1:p.Val227=
NM_001313913.2:c.565G= NP_001300842.1:p.Val189=