Canonical Allele Identifier: CA2466847961
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966098C= , CM000685.2:g.154966098C= GRCh38
NC_000023.10:g.154194373C= , CM000685.1:g.154194373C= GRCh37
NC_000023.9:g.153847567C= NCBI36
NG_011403.1:g.61626G=
NG_011403.2:g.61626G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1315G= MANE Select ENSP00000353393.4:p.Gly439=
ENST00000647125.1:c.*1191G= ENSP00000496062.1:n.*1191G=
ENST00000360256.8:c.1315G= ENSP00000353393.4:p.Gly439=
ENST00000483822.2:n.135G=
NM_000132.3:c.1315G= NP_000123.1:p.Gly439=
XM_011531126.1:c.1210G= XP_011529428.1:p.Gly404=
NM_000132.4:c.1315G= MANE Select NP_000123.1:p.Gly439=