Canonical Allele Identifier: CA2461412292
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562009G= , CM000685.2:g.139562009G= GRCh38
NC_000023.10:g.138644168G= , CM000685.1:g.138644168G= GRCh37
NC_000023.9:g.138471834G= NCBI36
NG_007994.1:g.36274G= , LRG_556:g.36274G=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1324G= MANE Select ENSP00000218099.2:p.Gly442=
ENST00000643157.1:n.1723+268G=
ENST00000218099.6:c.1324G= ENSP00000218099.2:p.Gly442=
ENST00000394090.2:c.1210G= ENSP00000377650.2:p.Gly404=
NM_000133.3:c.1324G= , LRG_556t1:c.1324G= NP_000124.1:p.Gly442=
NM_001313913.1:c.1210G= NP_001300842.1:p.Gly404=
XM_005262397.3:c.1195G= XP_005262454.1:p.Gly399=
XM_005262397.4:c.1195G= XP_005262454.1:p.Gly399=
NM_000133.4:c.1324G= MANE Select NP_000124.1:p.Gly442=
NM_001313913.2:c.1210G= NP_001300842.1:p.Gly404=