Canonical Allele Identifier: CA2466835698
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928486C= , CM000685.2:g.154928486C= GRCh38
NC_000023.10:g.154156761C= , CM000685.1:g.154156761C= GRCh37
NC_000023.9:g.153809955C= NCBI36
NG_011403.1:g.99238G=
NG_011403.2:g.99238G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5219+85G= MANE Select ENSP00000353393.4:n.5219+85G=
ENST00000360256.8:c.5219+85G= ENSP00000353393.4:n.5219+85G=
NM_000132.3:c.5219+85G= NP_000123.1:n.5219+85G=
XM_011531126.1:c.5114+85G= XP_011529428.1:n.5114+85G=
NM_000132.4:c.5219+85G= MANE Select NP_000123.1:n.5219+85G=
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