Canonical Allele Identifier: CA414917747
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969378T>A , CM000685.2:g.154969378T>A GRCh38
NC_000023.10:g.154197653T>A , CM000685.1:g.154197653T>A GRCh37
NC_000023.9:g.153850847T>A NCBI36
NG_011403.1:g.58346A>T
NG_011403.2:g.58346A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.962A>T MANE Select ENSP00000353393.4:p.Asp321Val
ENST00000647125.1:c.*838A>T ENSP00000496062.1:n.*838A>T
ENST00000360256.8:c.962A>T ENSP00000353393.4:p.Asp321Val
NM_000132.3:c.962A>T NP_000123.1:p.Asp321Val
XM_011531126.1:c.857A>T XP_011529428.1:p.Asp286Val
NM_000132.4:c.962A>T MANE Select NP_000123.1:p.Asp321Val