Canonical Allele Identifier: CA414912020
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957112T>G , CM000685.2:g.154957112T>G GRCh38
NC_000023.10:g.154185387T>G , CM000685.1:g.154185387T>G GRCh37
NC_000023.9:g.153838581T>G NCBI36
NG_011403.1:g.70612A>C
NG_011403.2:g.70612A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1597A>C MANE Select ENSP00000353393.4:p.Thr533Pro
ENST00000647125.1:c.*1473A>C ENSP00000496062.1:n.*1473A>C
ENST00000360256.8:c.1597A>C ENSP00000353393.4:p.Thr533Pro
NM_000132.3:c.1597A>C NP_000123.1:p.Thr533Pro
XM_011531126.1:c.1492A>C XP_011529428.1:p.Thr498Pro
NM_000132.4:c.1597A>C MANE Select NP_000123.1:p.Thr533Pro