Canonical Allele Identifier: CA2461412322
Gene: F9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562087C= , CM000685.2:g.139562087C= GRCh38
NC_000023.10:g.138644246C= , CM000685.1:g.138644246C= GRCh37
NC_000023.9:g.138471912C= NCBI36
NG_007994.1:g.36352C= , LRG_556:g.36352C=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.*16C= MANE Select ENSP00000218099.2:n.*16C=
ENST00000643157.1:n.1723+346C=
ENST00000218099.6:c.*16C= ENSP00000218099.2:n.*16C=
NM_000133.3:c.*16C= , LRG_556t1:c.*16C= NP_000124.1:n.*16C=
NM_001313913.1:c.*16C= NP_001300842.1:n.*16C=
XM_005262397.3:c.*16C= XP_005262454.1:n.*16C=
XM_005262397.4:c.*16C= XP_005262454.1:n.*16C=
NM_000133.4:c.*16C= MANE Select NP_000124.1:n.*16C=
NM_001313913.2:c.*16C= NP_001300842.1:n.*16C=
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