Canonical Allele Identifier: CA2466828447
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904907T= , CM000685.2:g.154904907T= GRCh38
NC_000023.10:g.154133182T= , CM000685.1:g.154133182T= GRCh37
NC_000023.9:g.153786376T= NCBI36
NG_011403.1:g.122817A=
NG_011403.2:g.122817A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5490A= MANE Select ENSP00000353393.4:p.Glu1830=
ENST00000360256.8:c.5490A= ENSP00000353393.4:p.Glu1830=
NM_000132.3:c.5490A= NP_000123.1:p.Glu1830=
XM_011531126.1:c.5385A= XP_011529428.1:p.Glu1795=
NM_000132.4:c.5490A= MANE Select NP_000123.1:p.Glu1830=
Search 100 bp 5'
Search 100 bp 3'