Canonical Allele Identifier: CA2466857792
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997065A= , CM000685.2:g.154997065A= GRCh38
NC_000023.10:g.154225340A= , CM000685.1:g.154225340A= GRCh37
NC_000023.9:g.153878534A= NCBI36
NG_011403.1:g.30659T=
NG_011403.2:g.30659T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.296T= MANE Select ENSP00000353393.4:p.Val99=
ENST00000647125.1:c.*82T= ENSP00000496062.1:n.*82T=
ENST00000360256.8:c.296T= ENSP00000353393.4:p.Val99=
ENST00000423959.5:c.191T= ENSP00000409446.1:p.Val64=
ENST00000453950.1:c.278T= ENSP00000389153.1:p.Val93=
NM_000132.3:c.296T= NP_000123.1:p.Val99=
XM_011531126.1:c.191T= XP_011529428.1:p.Val64=
NM_000132.4:c.296T= MANE Select NP_000123.1:p.Val99=