Canonical Allele Identifier: CA2466836660
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931350G= , CM000685.2:g.154931350G= GRCh38
NC_000023.10:g.154159625G= , CM000685.1:g.154159625G= GRCh37
NC_000023.9:g.153812819G= NCBI36
NG_011403.1:g.96374C=
NG_011403.2:g.96374C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.2440C= MANE Select ENSP00000353393.4:p.Arg814=
ENST00000647125.1:c.*2106C= ENSP00000496062.1:n.*2106C=
ENST00000360256.8:c.2440C= ENSP00000353393.4:p.Arg814=
NM_000132.3:c.2440C= NP_000123.1:p.Arg814=
XM_011531126.1:c.2335C= XP_011529428.1:p.Arg779=
NM_000132.4:c.2440C= MANE Select NP_000123.1:p.Arg814=