Canonical Allele Identifier: CA519365739
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs137852368

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966634G>T , CM000685.2:g.154966634G>T GRCh38
NC_000023.10:g.154194909G>T , CM000685.1:g.154194909G>T GRCh37
NC_000023.9:g.153848103G>T NCBI36
NG_011403.1:g.61090C>A
NG_011403.2:g.61090C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1063C>A MANE Select ENSP00000353393.4:p.Arg355=
ENST00000647125.1:c.*939C>A ENSP00000496062.1:n.*939C>A
ENST00000360256.8:c.1063C>A ENSP00000353393.4:p.Arg355=
NM_000132.3:c.1063C>A NP_000123.1:p.Arg355=
XM_011531126.1:c.958C>A XP_011529428.1:p.Arg320=
NM_000132.4:c.1063C>A MANE Select NP_000123.1:p.Arg355=