Canonical Allele Identifier: CA2466847919
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154965977G= , CM000685.2:g.154965977G= GRCh38
NC_000023.10:g.154194252G= , CM000685.1:g.154194252G= GRCh37
NC_000023.9:g.153847446G= NCBI36
NG_011403.1:g.61747C=
NG_011403.2:g.61747C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1436C= MANE Select ENSP00000353393.4:p.Thr479=
ENST00000647125.1:c.*1312C= ENSP00000496062.1:n.*1312C=
ENST00000360256.8:c.1436C= ENSP00000353393.4:p.Thr479=
ENST00000483822.2:n.256C=
NM_000132.3:c.1436C= NP_000123.1:p.Thr479=
XM_011531126.1:c.1331C= XP_011529428.1:p.Thr444=
NM_000132.4:c.1436C= MANE Select NP_000123.1:p.Thr479=