Canonical Allele Identifier: CA121128
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10591
dbSNP Id: rs137852241

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551218G>A , CM000685.2:g.139551218G>A GRCh38
NC_000023.10:g.138633377G>A , CM000685.1:g.138633377G>A GRCh37
NC_000023.9:g.138461043G>A NCBI36
NG_007994.1:g.25483G>A , LRG_556:g.25483G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.677G>A MANE Select ENSP00000218099.2:p.Arg226Gln
ENST00000643157.1:n.1344G>A
ENST00000218099.6:c.677G>A ENSP00000218099.2:p.Arg226Gln
ENST00000394090.2:c.563G>A ENSP00000377650.2:p.Arg188Gln
NM_000133.3:c.677G>A , LRG_556t1:c.677G>A NP_000124.1:p.Arg226Gln
NM_001313913.1:c.563G>A NP_001300842.1:p.Arg188Gln
XM_005262397.3:c.548G>A XP_005262454.1:p.Arg183Gln
XM_005262397.4:c.548G>A XP_005262454.1:p.Arg183Gln
NM_000133.4:c.677G>A MANE Select NP_000124.1:p.Arg226Gln
NM_001313913.2:c.563G>A NP_001300842.1:p.Arg188Gln