Canonical Allele Identifier: CA2466865488
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022660A= , CM000685.2:g.155022660A= GRCh38
NC_000023.10:g.154250935A= , CM000685.1:g.154250935A= GRCh37
NC_000023.9:g.153904129A= NCBI36
NG_011403.1:g.5064T=
NG_011403.2:g.5064T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.-108T= MANE Select ENSP00000353393.4:n.-108T=
ENST00000647125.1:c.-108T= ENSP00000496062.1:n.-108T=
ENST00000360256.8:c.-108T= ENSP00000353393.4:n.-108T=
ENST00000423959.5:c.38+4120T= ENSP00000409446.1:n.38+4120T=
ENST00000453950.1:c.39-164T= ENSP00000389153.1:n.39-164T=
NM_000132.3:c.-108T= NP_000123.1:n.-108T=
XM_011531126.1:c.38+4120T= XP_011529428.1:n.38+4120T=
NM_000132.4:c.-108T= MANE Select NP_000123.1:n.-108T=