Canonical Allele Identifier: CA2461412189
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561820C= , CM000685.2:g.139561820C= GRCh38
NC_000023.10:g.138643979C= , CM000685.1:g.138643979C= GRCh37
NC_000023.9:g.138471645C= NCBI36
NG_007994.1:g.36085C= , LRG_556:g.36085C=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1135C= MANE Select ENSP00000218099.2:p.Arg379=
ENST00000643157.1:n.1723+79C=
ENST00000218099.6:c.1135C= ENSP00000218099.2:p.Arg379=
ENST00000394090.2:c.1021C= ENSP00000377650.2:p.Arg341=
NM_000133.3:c.1135C= , LRG_556t1:c.1135C= NP_000124.1:p.Arg379=
NM_001313913.1:c.1021C= NP_001300842.1:p.Arg341=
XM_005262397.3:c.1006C= XP_005262454.1:p.Arg336=
XM_005262397.4:c.1006C= XP_005262454.1:p.Arg336=
NM_000133.4:c.1135C= MANE Select NP_000124.1:p.Arg379=
NM_001313913.2:c.1021C= NP_001300842.1:p.Arg341=