Canonical Allele Identifier: CA414437662
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139541145A>G , CM000685.2:g.139541145A>G GRCh38
NC_000023.10:g.138623304A>G , CM000685.1:g.138623304A>G GRCh37
NC_000023.9:g.138450970A>G NCBI36
NG_007994.1:g.15410A>G , LRG_556:g.15410A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.347A>G MANE Select ENSP00000218099.2:p.Glu116Gly
ENST00000218099.6:c.347A>G ENSP00000218099.2:p.Glu116Gly
ENST00000394090.2:c.277+3759A>G ENSP00000377650.2:n.277+3759A>G
ENST00000479617.2:n.300A>G
NM_000133.3:c.347A>G , LRG_556t1:c.347A>G NP_000124.1:p.Glu116Gly
NM_001313913.1:c.277+3759A>G NP_001300842.1:n.277+3759A>G
XM_005262397.3:c.347A>G XP_005262454.1:p.Glu116Gly
XM_005262397.4:c.347A>G XP_005262454.1:p.Glu116Gly
NM_000133.4:c.347A>G MANE Select NP_000124.1:p.Glu116Gly
NM_001313913.2:c.277+3759A>G NP_001300842.1:n.277+3759A>G