Canonical Allele Identifier: CA2466845351
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957073G= , CM000685.2:g.154957073G= GRCh38
NC_000023.10:g.154185348G= , CM000685.1:g.154185348G= GRCh37
NC_000023.9:g.153838542G= NCBI36
NG_011403.1:g.70651C=
NG_011403.2:g.70651C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1636C= MANE Select ENSP00000353393.4:p.Arg546=
ENST00000647125.1:c.*1512C= ENSP00000496062.1:n.*1512C=
ENST00000360256.8:c.1636C= ENSP00000353393.4:p.Arg546=
NM_000132.3:c.1636C= NP_000123.1:p.Arg546=
XM_011531126.1:c.1531C= XP_011529428.1:p.Arg511=
NM_000132.4:c.1636C= MANE Select NP_000123.1:p.Arg546=