Canonical Allele Identifier: CA2466848133
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966566G= , CM000685.2:g.154966566G= GRCh38
NC_000023.10:g.154194841G= , CM000685.1:g.154194841G= GRCh37
NC_000023.9:g.153848035G= NCBI36
NG_011403.1:g.61158C=
NG_011403.2:g.61158C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1131C= MANE Select ENSP00000353393.4:p.Val377=
ENST00000647125.1:c.*1007C= ENSP00000496062.1:n.*1007C=
ENST00000360256.8:c.1131C= ENSP00000353393.4:p.Val377=
NM_000132.3:c.1131C= NP_000123.1:p.Val377=
XM_011531126.1:c.1026C= XP_011529428.1:p.Val342=
NM_000132.4:c.1131C= MANE Select NP_000123.1:p.Val377=