Canonical Allele Identifier: CA414444733
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561591C>A , CM000685.2:g.139561591C>A GRCh38
NC_000023.10:g.138643750C>A , CM000685.1:g.138643750C>A GRCh37
NC_000023.9:g.138471416C>A NCBI36
NG_007994.1:g.35856C>A , LRG_556:g.35856C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.906C>A MANE Select ENSP00000218099.2:p.His302Gln
ENST00000643157.1:n.1573C>A
ENST00000218099.6:c.906C>A ENSP00000218099.2:p.His302Gln
ENST00000394090.2:c.792C>A ENSP00000377650.2:p.His264Gln
NM_000133.3:c.906C>A , LRG_556t1:c.906C>A NP_000124.1:p.His302Gln
NM_001313913.1:c.792C>A NP_001300842.1:p.His264Gln
XM_005262397.3:c.777C>A XP_005262454.1:p.His259Gln
XM_005262397.4:c.777C>A XP_005262454.1:p.His259Gln
NM_000133.4:c.906C>A MANE Select NP_000124.1:p.His302Gln
NM_001313913.2:c.792C>A NP_001300842.1:p.His264Gln