Canonical Allele Identifier: CA2466846477
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154961074C= , CM000685.2:g.154961074C= GRCh38
NC_000023.10:g.154189349C= , CM000685.1:g.154189349C= GRCh37
NC_000023.9:g.153842543C= NCBI36
NG_011403.1:g.66650G=
NG_011403.2:g.66650G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1537+1G= MANE Select ENSP00000353393.4:n.1537+1G=
ENST00000647125.1:c.*1413+1G= ENSP00000496062.1:n.*1413+1G=
ENST00000360256.8:c.1537+1G= ENSP00000353393.4:n.1537+1G=
NM_000132.3:c.1537+1G= NP_000123.1:n.1537+1G=
XM_011531126.1:c.1432+1G= XP_011529428.1:n.1432+1G=
NM_000132.4:c.1537+1G= MANE Select NP_000123.1:n.1537+1G=
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