Canonical Allele Identifier: CA2466857808
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997095C= , CM000685.2:g.154997095C= GRCh38
NC_000023.10:g.154225370C= , CM000685.1:g.154225370C= GRCh37
NC_000023.9:g.153878564C= NCBI36
NG_011403.1:g.30629G=
NG_011403.2:g.30629G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.266G= MANE Select ENSP00000353393.4:p.Gly89=
ENST00000647125.1:c.*52G= ENSP00000496062.1:n.*52G=
ENST00000360256.8:c.266G= ENSP00000353393.4:p.Gly89=
ENST00000423959.5:c.161G= ENSP00000409446.1:p.Gly54=
ENST00000453950.1:c.248G= ENSP00000389153.1:p.Gly83=
NM_000132.3:c.266G= NP_000123.1:p.Gly89=
XM_011531126.1:c.161G= XP_011529428.1:p.Gly54=
NM_000132.4:c.266G= MANE Select NP_000123.1:p.Gly89=