Canonical Allele Identifier: CA2466835814
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928807G= , CM000685.2:g.154928807G= GRCh38
NC_000023.10:g.154157082G= , CM000685.1:g.154157082G= GRCh37
NC_000023.9:g.153810276G= NCBI36
NG_011403.1:g.98917C=
NG_011403.2:g.98917C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4983C= MANE Select ENSP00000353393.4:p.Val1661=
ENST00000360256.8:c.4983C= ENSP00000353393.4:p.Val1661=
NM_000132.3:c.4983C= NP_000123.1:p.Val1661=
XM_011531126.1:c.4878C= XP_011529428.1:p.Val1626=
NM_000132.4:c.4983C= MANE Select NP_000123.1:p.Val1661=