Canonical Allele Identifier: CA2461412058
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561500T= , CM000685.2:g.139561500T= GRCh38
NC_000023.10:g.138643659T= , CM000685.1:g.138643659T= GRCh37
NC_000023.9:g.138471325T= NCBI36
NG_007994.1:g.35765T= , LRG_556:g.35765T=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.839-24T= MANE Select ENSP00000218099.2:n.839-24T=
ENST00000643157.1:n.1506-24T=
ENST00000218099.6:c.839-24T= ENSP00000218099.2:n.839-24T=
ENST00000394090.2:c.725-24T= ENSP00000377650.2:n.725-24T=
NM_000133.3:c.839-24T= , LRG_556t1:c.839-24T= NP_000124.1:n.839-24T=
NM_001313913.1:c.725-24T= NP_001300842.1:n.725-24T=
XM_005262397.3:c.710-24T= XP_005262454.1:n.710-24T=
XM_005262397.4:c.710-24T= XP_005262454.1:n.710-24T=
NM_000133.4:c.839-24T= MANE Select NP_000124.1:n.839-24T=
NM_001313913.2:c.725-24T= NP_001300842.1:n.725-24T=