Canonical Allele Identifier: CA414916601
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966558T>A , CM000685.2:g.154966558T>A GRCh38
NC_000023.10:g.154194833T>A , CM000685.1:g.154194833T>A GRCh37
NC_000023.9:g.153848027T>A NCBI36
NG_011403.1:g.61166A>T
NG_011403.2:g.61166A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1139A>T MANE Select ENSP00000353393.4:p.Asp380Val
ENST00000647125.1:c.*1015A>T ENSP00000496062.1:n.*1015A>T
ENST00000360256.8:c.1139A>T ENSP00000353393.4:p.Asp380Val
NM_000132.3:c.1139A>T NP_000123.1:p.Asp380Val
XM_011531126.1:c.1034A>T XP_011529428.1:p.Asp345Val
NM_000132.4:c.1139A>T MANE Select NP_000123.1:p.Asp380Val