Canonical Allele Identifier: CA2466856487
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154992931C= , CM000685.2:g.154992931C= GRCh38
NC_000023.10:g.154221206C= , CM000685.1:g.154221206C= GRCh37
NC_000023.9:g.153874400C= NCBI36
NG_011403.1:g.34793G=
NG_011403.2:g.34793G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.601+5G= MANE Select ENSP00000353393.4:n.601+5G=
ENST00000647125.1:c.*387+5G= ENSP00000496062.1:n.*387+5G=
ENST00000360256.8:c.601+5G= ENSP00000353393.4:n.601+5G=
ENST00000423959.5:c.496+5G= ENSP00000409446.1:n.496+5G=
NM_000132.3:c.601+5G= NP_000123.1:n.601+5G=
XM_011531126.1:c.496+5G= XP_011529428.1:n.496+5G=
NM_000132.4:c.601+5G= MANE Select NP_000123.1:n.601+5G=
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