Canonical Allele Identifier: CA2461407753
Gene: F9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139548321C= , CM000685.2:g.139548321C= GRCh38
NC_000023.10:g.138630480C= , CM000685.1:g.138630480C= GRCh37
NC_000023.9:g.138458146C= NCBI36
NG_007994.1:g.22586C= , LRG_556:g.22586C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.392-42C= MANE Select ENSP00000218099.2:n.392-42C=
ENST00000643157.1:n.1059-42C=
ENST00000218099.6:c.392-42C= ENSP00000218099.2:n.392-42C=
ENST00000394090.2:c.278-42C= ENSP00000377650.2:n.278-42C=
ENST00000479617.2:n.345-42C=
NM_000133.3:c.392-42C= , LRG_556t1:c.392-42C= NP_000124.1:n.392-42C=
NM_001313913.1:c.278-42C= NP_001300842.1:n.278-42C=
XM_005262397.3:c.392-2741C= XP_005262454.1:n.392-2741C=
XM_005262397.4:c.392-2741C= XP_005262454.1:n.392-2741C=
NM_000133.4:c.392-42C= MANE Select NP_000124.1:n.392-42C=
NM_001313913.2:c.278-42C= NP_001300842.1:n.278-42C=
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