Canonical Allele Identifier: CA336136040
Gene: F9 HGNC NCBI

Linked Data

dbSNP Id: rs104894807

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139548404T>C , CM000685.2:g.139548404T>C GRCh38
NC_000023.10:g.138630563T>C , CM000685.1:g.138630563T>C GRCh37
NC_000023.9:g.138458229T>C NCBI36
NG_007994.1:g.22669T>C , LRG_556:g.22669T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.433T>C MANE Select ENSP00000218099.2:p.Cys145Arg
ENST00000643157.1:n.1100T>C
ENST00000218099.6:c.433T>C ENSP00000218099.2:p.Cys145Arg
ENST00000394090.2:c.319T>C ENSP00000377650.2:p.Cys107Arg
NM_000133.3:c.433T>C , LRG_556t1:c.433T>C NP_000124.1:p.Cys145Arg
NM_001313913.1:c.319T>C NP_001300842.1:p.Cys107Arg
XM_005262397.3:c.392-2658T>C XP_005262454.1:n.392-2658T>C
XM_005262397.4:c.392-2658T>C XP_005262454.1:n.392-2658T>C
NM_000133.4:c.433T>C MANE Select NP_000124.1:p.Cys145Arg
NM_001313913.2:c.319T>C NP_001300842.1:p.Cys107Arg