Canonical Allele Identifier: CA2466842808
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154948680T= , CM000685.2:g.154948680T= GRCh38
NC_000023.10:g.154176955T= , CM000685.1:g.154176955T= GRCh37
NC_000023.9:g.153830149T= NCBI36
NG_011403.1:g.79044A=
NG_011403.2:g.79044A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1904-773A= MANE Select ENSP00000353393.4:n.1904-773A=
ENST00000647125.1:c.*1779+5212A= ENSP00000496062.1:n.*1779+5212A=
ENST00000360256.8:c.1904-773A= ENSP00000353393.4:n.1904-773A=
NM_000132.3:c.1904-773A= NP_000123.1:n.1904-773A=
XM_011531126.1:c.1799-773A= XP_011529428.1:n.1799-773A=
NM_000132.4:c.1904-773A= MANE Select NP_000123.1:n.1904-773A=
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