Canonical Allele Identifier: CA414917741
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969376G>T , CM000685.2:g.154969376G>T GRCh38
NC_000023.10:g.154197651G>T , CM000685.1:g.154197651G>T GRCh37
NC_000023.9:g.153850845G>T NCBI36
NG_011403.1:g.58348C>A
NG_011403.2:g.58348C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.964C>A MANE Select ENSP00000353393.4:p.Leu322Ile
ENST00000647125.1:c.*840C>A ENSP00000496062.1:n.*840C>A
ENST00000360256.8:c.964C>A ENSP00000353393.4:p.Leu322Ile
NM_000132.3:c.964C>A NP_000123.1:p.Leu322Ile
XM_011531126.1:c.859C>A XP_011529428.1:p.Leu287Ile
NM_000132.4:c.964C>A MANE Select NP_000123.1:p.Leu322Ile