Canonical Allele Identifier: CA2461407724
Gene: F9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139548238C= , CM000685.2:g.139548238C= GRCh38
NC_000023.10:g.138630397C= , CM000685.1:g.138630397C= GRCh37
NC_000023.9:g.138458063C= NCBI36
NG_007994.1:g.22503C= , LRG_556:g.22503C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.392-125C= MANE Select ENSP00000218099.2:n.392-125C=
ENST00000643157.1:n.1059-125C=
ENST00000218099.6:c.392-125C= ENSP00000218099.2:n.392-125C=
ENST00000394090.2:c.278-125C= ENSP00000377650.2:n.278-125C=
ENST00000479617.2:n.345-125C=
NM_000133.3:c.392-125C= , LRG_556t1:c.392-125C= NP_000124.1:n.392-125C=
NM_001313913.1:c.278-125C= NP_001300842.1:n.278-125C=
XM_005262397.3:c.392-2824C= XP_005262454.1:n.392-2824C=
XM_005262397.4:c.392-2824C= XP_005262454.1:n.392-2824C=
NM_000133.4:c.392-125C= MANE Select NP_000124.1:n.392-125C=
NM_001313913.2:c.278-125C= NP_001300842.1:n.278-125C=
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