Canonical Allele Identifier: CA2461412191
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561827C= , CM000685.2:g.139561827C= GRCh38
NC_000023.10:g.138643986C= , CM000685.1:g.138643986C= GRCh37
NC_000023.9:g.138471652C= NCBI36
NG_007994.1:g.36092C= , LRG_556:g.36092C=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1142C= MANE Select ENSP00000218099.2:p.Thr381=
ENST00000643157.1:n.1723+86C=
ENST00000218099.6:c.1142C= ENSP00000218099.2:p.Thr381=
ENST00000394090.2:c.1028C= ENSP00000377650.2:p.Thr343=
NM_000133.3:c.1142C= , LRG_556t1:c.1142C= NP_000124.1:p.Thr381=
NM_001313913.1:c.1028C= NP_001300842.1:p.Thr343=
XM_005262397.3:c.1013C= XP_005262454.1:p.Thr338=
XM_005262397.4:c.1013C= XP_005262454.1:p.Thr338=
NM_000133.4:c.1142C= MANE Select NP_000124.1:p.Thr381=
NM_001313913.2:c.1028C= NP_001300842.1:p.Thr343=