Canonical Allele Identifier: CA10529811
Gene: F9 HGNC NCBI

Linked Data

dbSNP Id: rs756270566

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551118G>A , CM000685.2:g.139551118G>A GRCh38
NC_000023.10:g.138633277G>A , CM000685.1:g.138633277G>A GRCh37
NC_000023.9:g.138460943G>A NCBI36
NG_007994.1:g.25383G>A , LRG_556:g.25383G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.577G>A MANE Select ENSP00000218099.2:p.Glu193Lys
ENST00000643157.1:n.1244G>A
ENST00000218099.6:c.577G>A ENSP00000218099.2:p.Glu193Lys
ENST00000394090.2:c.463G>A ENSP00000377650.2:p.Glu155Lys
NM_000133.3:c.577G>A , LRG_556t1:c.577G>A NP_000124.1:p.Glu193Lys
NM_001313913.1:c.463G>A NP_001300842.1:p.Glu155Lys
XM_005262397.3:c.448G>A XP_005262454.1:p.Glu150Lys
XM_005262397.4:c.448G>A XP_005262454.1:p.Glu150Lys
NM_000133.4:c.577G>A MANE Select NP_000124.1:p.Glu193Lys
NM_001313913.2:c.463G>A NP_001300842.1:p.Glu155Lys