Canonical Allele Identifier: CA2461412293
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562010G= , CM000685.2:g.139562010G= GRCh38
NC_000023.10:g.138644169G= , CM000685.1:g.138644169G= GRCh37
NC_000023.9:g.138471835G= NCBI36
NG_007994.1:g.36275G= , LRG_556:g.36275G=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1325G= MANE Select ENSP00000218099.2:p.Gly442=
ENST00000643157.1:n.1723+269G=
ENST00000218099.6:c.1325G= ENSP00000218099.2:p.Gly442=
ENST00000394090.2:c.1211G= ENSP00000377650.2:p.Gly404=
NM_000133.3:c.1325G= , LRG_556t1:c.1325G= NP_000124.1:p.Gly442=
NM_001313913.1:c.1211G= NP_001300842.1:p.Gly404=
XM_005262397.3:c.1196G= XP_005262454.1:p.Gly399=
XM_005262397.4:c.1196G= XP_005262454.1:p.Gly399=
NM_000133.4:c.1325G= MANE Select NP_000124.1:p.Gly442=
NM_001313913.2:c.1211G= NP_001300842.1:p.Gly404=