Canonical Allele Identifier: CA2466827589
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154901933T= , CM000685.2:g.154901933T= GRCh38
NC_000023.10:g.154130208T= , CM000685.1:g.154130208T= GRCh37
NC_000023.9:g.153783402T= NCBI36
NG_011403.1:g.125791A=
NG_011403.2:g.125791A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6115+118A= MANE Select ENSP00000353393.4:n.6115+118A=
ENST00000360256.8:c.6115+118A= ENSP00000353393.4:n.6115+118A=
NM_000132.3:c.6115+118A= NP_000123.1:n.6115+118A=
XM_011531126.1:c.6010+118A= XP_011529428.1:n.6010+118A=
NM_000132.4:c.6115+118A= MANE Select NP_000123.1:n.6115+118A=
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