Canonical Allele Identifier: CA2466828460
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904944C= , CM000685.2:g.154904944C= GRCh38
NC_000023.10:g.154133219C= , CM000685.1:g.154133219C= GRCh37
NC_000023.9:g.153786413C= NCBI36
NG_011403.1:g.122780G=
NG_011403.2:g.122780G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5453G= MANE Select ENSP00000353393.4:p.Gly1818=
ENST00000360256.8:c.5453G= ENSP00000353393.4:p.Gly1818=
NM_000132.3:c.5453G= NP_000123.1:p.Gly1818=
XM_011531126.1:c.5348G= XP_011529428.1:p.Gly1783=
NM_000132.4:c.5453G= MANE Select NP_000123.1:p.Gly1818=