Canonical Allele Identifier: CA414446163
Gene: F9 HGNC NCBI

Linked Data

dbSNP Id: rs1303221289

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561830G>A , CM000685.2:g.139561830G>A GRCh38
NC_000023.10:g.138643989G>A , CM000685.1:g.138643989G>A GRCh37
NC_000023.9:g.138471655G>A NCBI36
NG_007994.1:g.36095G>A , LRG_556:g.36095G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1145G>A MANE Select ENSP00000218099.2:p.Cys382Tyr
ENST00000643157.1:n.1723+89G>A
ENST00000218099.6:c.1145G>A ENSP00000218099.2:p.Cys382Tyr
ENST00000394090.2:c.1031G>A ENSP00000377650.2:p.Cys344Tyr
NM_000133.3:c.1145G>A , LRG_556t1:c.1145G>A NP_000124.1:p.Cys382Tyr
NM_001313913.1:c.1031G>A NP_001300842.1:p.Cys344Tyr
XM_005262397.3:c.1016G>A XP_005262454.1:p.Cys339Tyr
XM_005262397.4:c.1016G>A XP_005262454.1:p.Cys339Tyr
NM_000133.4:c.1145G>A MANE Select NP_000124.1:p.Cys382Tyr
NM_001313913.2:c.1031G>A NP_001300842.1:p.Cys344Tyr