Canonical Allele Identifier: CA2466848981
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969370G= , CM000685.2:g.154969370G= GRCh38
NC_000023.10:g.154197645G= , CM000685.1:g.154197645G= GRCh37
NC_000023.9:g.153850839G= NCBI36
NG_011403.1:g.58354C=
NG_011403.2:g.58354C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.970C= MANE Select ENSP00000353393.4:p.Gln324=
ENST00000647125.1:c.*846C= ENSP00000496062.1:n.*846C=
ENST00000360256.8:c.970C= ENSP00000353393.4:p.Gln324=
NM_000132.3:c.970C= NP_000123.1:p.Gln324=
XM_011531126.1:c.865C= XP_011529428.1:p.Gln289=
NM_000132.4:c.970C= MANE Select NP_000123.1:p.Gln324=