Canonical Allele Identifier: CA2461412317
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562072T= , CM000685.2:g.139562072T= GRCh38
NC_000023.10:g.138644231T= , CM000685.1:g.138644231T= GRCh37
NC_000023.9:g.138471897T= NCBI36
NG_007994.1:g.36337T= , LRG_556:g.36337T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.*1T= MANE Select ENSP00000218099.2:n.*1T=
ENST00000643157.1:n.1723+331T=
ENST00000218099.6:c.*1T= ENSP00000218099.2:n.*1T=
NM_000133.3:c.*1T= , LRG_556t1:c.*1T= NP_000124.1:n.*1T=
NM_001313913.1:c.*1T= NP_001300842.1:n.*1T=
XM_005262397.3:c.*1T= XP_005262454.1:n.*1T=
XM_005262397.4:c.*1T= XP_005262454.1:n.*1T=
NM_000133.4:c.*1T= MANE Select NP_000124.1:n.*1T=
NM_001313913.2:c.*1T= NP_001300842.1:n.*1T=