Canonical Allele Identifier: CA2461412320
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562078A= , CM000685.2:g.139562078A= GRCh38
NC_000023.10:g.138644237A= , CM000685.1:g.138644237A= GRCh37
NC_000023.9:g.138471903A= NCBI36
NG_007994.1:g.36343A= , LRG_556:g.36343A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.*7A= MANE Select ENSP00000218099.2:n.*7A=
ENST00000643157.1:n.1723+337A=
ENST00000218099.6:c.*7A= ENSP00000218099.2:n.*7A=
NM_000133.3:c.*7A= , LRG_556t1:c.*7A= NP_000124.1:n.*7A=
NM_001313913.1:c.*7A= NP_001300842.1:n.*7A=
XM_005262397.3:c.*7A= XP_005262454.1:n.*7A=
XM_005262397.4:c.*7A= XP_005262454.1:n.*7A=
NM_000133.4:c.*7A= MANE Select NP_000124.1:n.*7A=
NM_001313913.2:c.*7A= NP_001300842.1:n.*7A=