Canonical Allele Identifier: CA2461412329
Gene: F9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562100T= , CM000685.2:g.139562100T= GRCh38
NC_000023.10:g.138644259T= , CM000685.1:g.138644259T= GRCh37
NC_000023.9:g.138471925T= NCBI36
NG_007994.1:g.36365T= , LRG_556:g.36365T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.*29T= MANE Select ENSP00000218099.2:n.*29T=
ENST00000643157.1:n.1723+359T=
ENST00000218099.6:c.*29T= ENSP00000218099.2:n.*29T=
NM_000133.3:c.*29T= , LRG_556t1:c.*29T= NP_000124.1:n.*29T=
NM_001313913.1:c.*29T= NP_001300842.1:n.*29T=
XM_005262397.3:c.*29T= XP_005262454.1:n.*29T=
XM_005262397.4:c.*29T= XP_005262454.1:n.*29T=
NM_000133.4:c.*29T= MANE Select NP_000124.1:n.*29T=
NM_001313913.2:c.*29T= NP_001300842.1:n.*29T=
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