Canonical Allele Identifier: CA414913705
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928637A>T , CM000685.2:g.154928637A>T GRCh38
NC_000023.10:g.154156912A>T , CM000685.1:g.154156912A>T GRCh37
NC_000023.9:g.153810106A>T NCBI36
NG_011403.1:g.99087T>A
NG_011403.2:g.99087T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5153T>A MANE Select ENSP00000353393.4:p.Phe1718Tyr
ENST00000360256.8:c.5153T>A ENSP00000353393.4:p.Phe1718Tyr
NM_000132.3:c.5153T>A NP_000123.1:p.Phe1718Tyr
XM_011531126.1:c.5048T>A XP_011529428.1:p.Phe1683Tyr
NM_000132.4:c.5153T>A MANE Select NP_000123.1:p.Phe1718Tyr