Canonical Allele Identifier: CA2466847897
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154965902A= , CM000685.2:g.154965902A= GRCh38
NC_000023.10:g.154194177A= , CM000685.1:g.154194177A= GRCh37
NC_000023.9:g.153847371A= NCBI36
NG_011403.1:g.61822T=
NG_011403.2:g.61822T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1443+68T= MANE Select ENSP00000353393.4:n.1443+68T=
ENST00000647125.1:c.*1319+68T= ENSP00000496062.1:n.*1319+68T=
ENST00000360256.8:c.1443+68T= ENSP00000353393.4:n.1443+68T=
ENST00000483822.2:n.331T=
NM_000132.3:c.1443+68T= NP_000123.1:n.1443+68T=
XM_011531126.1:c.1338+68T= XP_011529428.1:n.1338+68T=
NM_000132.4:c.1443+68T= MANE Select NP_000123.1:n.1443+68T=