Canonical Allele Identifier: CA10529884
Gene: F9 HGNC NCBI

Linked Data

dbSNP Id: rs769009650

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561950C>T , CM000685.2:g.139561950C>T GRCh38
NC_000023.10:g.138644109C>T , CM000685.1:g.138644109C>T GRCh37
NC_000023.9:g.138471775C>T NCBI36
NG_007994.1:g.36215C>T , LRG_556:g.36215C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1265C>T MANE Select ENSP00000218099.2:p.Thr422Ile
ENST00000643157.1:n.1723+209C>T
ENST00000218099.6:c.1265C>T ENSP00000218099.2:p.Thr422Ile
ENST00000394090.2:c.1151C>T ENSP00000377650.2:p.Thr384Ile
NM_000133.3:c.1265C>T , LRG_556t1:c.1265C>T NP_000124.1:p.Thr422Ile
NM_001313913.1:c.1151C>T NP_001300842.1:p.Thr384Ile
XM_005262397.3:c.1136C>T XP_005262454.1:p.Thr379Ile
XM_005262397.4:c.1136C>T XP_005262454.1:p.Thr379Ile
NM_000133.4:c.1265C>T MANE Select NP_000124.1:p.Thr422Ile
NM_001313913.2:c.1151C>T NP_001300842.1:p.Thr384Ile