Canonical Allele Identifier: CA2461412070
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561529C= , CM000685.2:g.139561529C= GRCh38
NC_000023.10:g.138643688C= , CM000685.1:g.138643688C= GRCh37
NC_000023.9:g.138471354C= NCBI36
NG_007994.1:g.35794C= , LRG_556:g.35794C=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.844C= MANE Select ENSP00000218099.2:p.His282=
ENST00000643157.1:n.1511C=
ENST00000218099.6:c.844C= ENSP00000218099.2:p.His282=
ENST00000394090.2:c.730C= ENSP00000377650.2:p.His244=
NM_000133.3:c.844C= , LRG_556t1:c.844C= NP_000124.1:p.His282=
NM_001313913.1:c.730C= NP_001300842.1:p.His244=
XM_005262397.3:c.715C= XP_005262454.1:p.His239=
XM_005262397.4:c.715C= XP_005262454.1:p.His239=
NM_000133.4:c.844C= MANE Select NP_000124.1:p.His282=
NM_001313913.2:c.730C= NP_001300842.1:p.His244=