Canonical Allele Identifier: CA2461412269
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561956T= , CM000685.2:g.139561956T= GRCh38
NC_000023.10:g.138644115T= , CM000685.1:g.138644115T= GRCh37
NC_000023.9:g.138471781T= NCBI36
NG_007994.1:g.36221T= , LRG_556:g.36221T=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1271T= MANE Select ENSP00000218099.2:p.Phe424=
ENST00000643157.1:n.1723+215T=
ENST00000218099.6:c.1271T= ENSP00000218099.2:p.Phe424=
ENST00000394090.2:c.1157T= ENSP00000377650.2:p.Phe386=
NM_000133.3:c.1271T= , LRG_556t1:c.1271T= NP_000124.1:p.Phe424=
NM_001313913.1:c.1157T= NP_001300842.1:p.Phe386=
XM_005262397.3:c.1142T= XP_005262454.1:p.Phe381=
XM_005262397.4:c.1142T= XP_005262454.1:p.Phe381=
NM_000133.4:c.1271T= MANE Select NP_000124.1:p.Phe424=
NM_001313913.2:c.1157T= NP_001300842.1:p.Phe386=