Canonical Allele Identifier: CA414911311
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154954041A>T , CM000685.2:g.154954041A>T GRCh38
NC_000023.10:g.154182316A>T , CM000685.1:g.154182316A>T GRCh37
NC_000023.9:g.153835510A>T NCBI36
NG_011403.1:g.73683T>A
NG_011403.2:g.73683T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1754T>A MANE Select ENSP00000353393.4:p.Ile585Lys
ENST00000647125.1:c.*1630T>A ENSP00000496062.1:n.*1630T>A
ENST00000360256.8:c.1754T>A ENSP00000353393.4:p.Ile585Lys
NM_000132.3:c.1754T>A NP_000123.1:p.Ile585Lys
XM_011531126.1:c.1649T>A XP_011529428.1:p.Ile550Lys
NM_000132.4:c.1754T>A MANE Select NP_000123.1:p.Ile585Lys