Canonical Allele Identifier: CA414446966
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561955T>A , CM000685.2:g.139561955T>A GRCh38
NC_000023.10:g.138644114T>A , CM000685.1:g.138644114T>A GRCh37
NC_000023.9:g.138471780T>A NCBI36
NG_007994.1:g.36220T>A , LRG_556:g.36220T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1270T>A MANE Select ENSP00000218099.2:p.Phe424Ile
ENST00000643157.1:n.1723+214T>A
ENST00000218099.6:c.1270T>A ENSP00000218099.2:p.Phe424Ile
ENST00000394090.2:c.1156T>A ENSP00000377650.2:p.Phe386Ile
NM_000133.3:c.1270T>A , LRG_556t1:c.1270T>A NP_000124.1:p.Phe424Ile
NM_001313913.1:c.1156T>A NP_001300842.1:p.Phe386Ile
XM_005262397.3:c.1141T>A XP_005262454.1:p.Phe381Ile
XM_005262397.4:c.1141T>A XP_005262454.1:p.Phe381Ile
NM_000133.4:c.1270T>A MANE Select NP_000124.1:p.Phe424Ile
NM_001313913.2:c.1156T>A NP_001300842.1:p.Phe386Ile