Canonical Allele Identifier: CA2461412056
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561496G= , CM000685.2:g.139561496G= GRCh38
NC_000023.10:g.138643655G= , CM000685.1:g.138643655G= GRCh37
NC_000023.9:g.138471321G= NCBI36
NG_007994.1:g.35761G= , LRG_556:g.35761G=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.839-28G= MANE Select ENSP00000218099.2:n.839-28G=
ENST00000643157.1:n.1506-28G=
ENST00000218099.6:c.839-28G= ENSP00000218099.2:n.839-28G=
ENST00000394090.2:c.725-28G= ENSP00000377650.2:n.725-28G=
NM_000133.3:c.839-28G= , LRG_556t1:c.839-28G= NP_000124.1:n.839-28G=
NM_001313913.1:c.725-28G= NP_001300842.1:n.725-28G=
XM_005262397.3:c.710-28G= XP_005262454.1:n.710-28G=
XM_005262397.4:c.710-28G= XP_005262454.1:n.710-28G=
NM_000133.4:c.839-28G= MANE Select NP_000124.1:n.839-28G=
NM_001313913.2:c.725-28G= NP_001300842.1:n.725-28G=