Canonical Allele Identifier: CA255420
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10627
ClinVar RCV Id: RCV000011371
dbSNP Id: rs137852268

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562013T>C , CM000685.2:g.139562013T>C GRCh38
NC_000023.10:g.138644172T>C , CM000685.1:g.138644172T>C GRCh37
NC_000023.9:g.138471838T>C NCBI36
NG_007994.1:g.36278T>C , LRG_556:g.36278T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1328T>C MANE Select ENSP00000218099.2:p.Ile443Thr
ENST00000643157.1:n.1723+272T>C
ENST00000218099.6:c.1328T>C ENSP00000218099.2:p.Ile443Thr
ENST00000394090.2:n.1214T>C ENSP00000377650.2:p.Ile405Thr
NM_000133.3:c.1328T>C , LRG_556t1:c.1328T>C NP_000124.1:p.Ile443Thr
NM_001313913.1:c.1214T>C NP_001300842.1:p.Ile405Thr
XM_005262397.3:c.1199T>C XP_005262454.1:p.Ile400Thr
XM_005262397.4:c.1199T>C XP_005262454.1:p.Ile400Thr
NM_000133.4:c.1328T>C MANE Select NP_000124.1:p.Ile443Thr
NM_001313913.2:c.1214T>C NP_001300842.1:p.Ile405Thr