Canonical Allele Identifier: CA414902509
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931506A>T , CM000685.2:g.154931506A>T GRCh38
NC_000023.10:g.154159781A>T , CM000685.1:g.154159781A>T GRCh37
NC_000023.9:g.153812975A>T NCBI36
NG_011403.1:g.96218T>A
NG_011403.2:g.96218T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.2284T>A MANE Select ENSP00000353393.4:p.Ser762Thr
ENST00000647125.1:c.*1950T>A ENSP00000496062.1:n.*1950T>A
ENST00000360256.8:c.2284T>A ENSP00000353393.4:p.Ser762Thr
NM_000132.3:c.2284T>A NP_000123.1:p.Ser762Thr
XM_011531126.1:c.2179T>A XP_011529428.1:p.Ser727Thr
NM_000132.4:c.2284T>A MANE Select NP_000123.1:p.Ser762Thr