Canonical Allele Identifier: CA2466828464
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904956T= , CM000685.2:g.154904956T= GRCh38
NC_000023.10:g.154133231T= , CM000685.1:g.154133231T= GRCh37
NC_000023.9:g.153786425T= NCBI36
NG_011403.1:g.122768A=
NG_011403.2:g.122768A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5441A= MANE Select ENSP00000353393.4:p.Asp1814=
ENST00000360256.8:c.5441A= ENSP00000353393.4:p.Asp1814=
NM_000132.3:c.5441A= NP_000123.1:p.Asp1814=
XM_011531126.1:c.5336A= XP_011529428.1:p.Asp1779=
NM_000132.4:c.5441A= MANE Select NP_000123.1:p.Asp1814=