Canonical Allele Identifier: CA2466857799
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997079G= , CM000685.2:g.154997079G= GRCh38
NC_000023.10:g.154225354G= , CM000685.1:g.154225354G= GRCh37
NC_000023.9:g.153878548G= NCBI36
NG_011403.1:g.30645C=
NG_011403.2:g.30645C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.282C= MANE Select ENSP00000353393.4:p.Thr94=
ENST00000647125.1:c.*68C= ENSP00000496062.1:n.*68C=
ENST00000360256.8:c.282C= ENSP00000353393.4:p.Thr94=
ENST00000423959.5:c.177C= ENSP00000409446.1:p.Thr59=
ENST00000453950.1:c.264C= ENSP00000389153.1:p.Thr88=
NM_000132.3:c.282C= NP_000123.1:p.Thr94=
XM_011531126.1:c.177C= XP_011529428.1:p.Thr59=
NM_000132.4:c.282C= MANE Select NP_000123.1:p.Thr94=