Canonical Allele Identifier: CA2466848128
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966558T= , CM000685.2:g.154966558T= GRCh38
NC_000023.10:g.154194833T= , CM000685.1:g.154194833T= GRCh37
NC_000023.9:g.153848027T= NCBI36
NG_011403.1:g.61166A=
NG_011403.2:g.61166A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1139A= MANE Select ENSP00000353393.4:p.Asp380=
ENST00000647125.1:c.*1015A= ENSP00000496062.1:n.*1015A=
ENST00000360256.8:c.1139A= ENSP00000353393.4:p.Asp380=
NM_000132.3:c.1139A= NP_000123.1:p.Asp380=
XM_011531126.1:c.1034A= XP_011529428.1:p.Asp345=
NM_000132.4:c.1139A= MANE Select NP_000123.1:p.Asp380=