Canonical Allele Identifier: CA2466857782
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997043T= , CM000685.2:g.154997043T= GRCh38
NC_000023.10:g.154225318T= , CM000685.1:g.154225318T= GRCh37
NC_000023.9:g.153878512T= NCBI36
NG_011403.1:g.30681A=
NG_011403.2:g.30681A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.318A= MANE Select ENSP00000353393.4:p.Thr106=
ENST00000647125.1:c.*104A= ENSP00000496062.1:n.*104A=
ENST00000360256.8:c.318A= ENSP00000353393.4:p.Thr106=
ENST00000423959.5:c.213A= ENSP00000409446.1:p.Thr71=
ENST00000453950.1:c.300A= ENSP00000389153.1:p.Thr100=
NM_000132.3:c.318A= NP_000123.1:p.Thr106=
XM_011531126.1:c.213A= XP_011529428.1:p.Thr71=
NM_000132.4:c.318A= MANE Select NP_000123.1:p.Thr106=