Canonical Allele Identifier: CA2461412330
Gene: F9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562103G= , CM000685.2:g.139562103G= GRCh38
NC_000023.10:g.138644262G= , CM000685.1:g.138644262G= GRCh37
NC_000023.9:g.138471928G= NCBI36
NG_007994.1:g.36368G= , LRG_556:g.36368G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.*32G= MANE Select ENSP00000218099.2:n.*32G=
ENST00000643157.1:n.1723+362G=
ENST00000218099.6:c.*32G= ENSP00000218099.2:n.*32G=
NM_000133.3:c.*32G= , LRG_556t1:c.*32G= NP_000124.1:n.*32G=
NM_001313913.1:c.*32G= NP_001300842.1:n.*32G=
XM_005262397.3:c.*32G= XP_005262454.1:n.*32G=
XM_005262397.4:c.*32G= XP_005262454.1:n.*32G=
NM_000133.4:c.*32G= MANE Select NP_000124.1:n.*32G=
NM_001313913.2:c.*32G= NP_001300842.1:n.*32G=
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