Canonical Allele Identifier: CA2466847950
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966065A= , CM000685.2:g.154966065A= GRCh38
NC_000023.10:g.154194340A= , CM000685.1:g.154194340A= GRCh37
NC_000023.9:g.153847534A= NCBI36
NG_011403.1:g.61659T=
NG_011403.2:g.61659T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1348T= MANE Select ENSP00000353393.4:p.Tyr450=
ENST00000647125.1:c.*1224T= ENSP00000496062.1:n.*1224T=
ENST00000360256.8:c.1348T= ENSP00000353393.4:p.Tyr450=
ENST00000483822.2:n.168T=
NM_000132.3:c.1348T= NP_000123.1:p.Tyr450=
XM_011531126.1:c.1243T= XP_011529428.1:p.Tyr415=
NM_000132.4:c.1348T= MANE Select NP_000123.1:p.Tyr450=