Canonical Allele Identifier: CA414920439
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022415G>T , CM000685.2:g.155022415G>T GRCh38
NC_000023.10:g.154250690G>T , CM000685.1:g.154250690G>T GRCh37
NC_000023.9:g.153903884G>T NCBI36
NG_011403.1:g.5309C>A
NG_011403.2:g.5309C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.138C>A MANE Select ENSP00000353393.4:p.Asp46Glu
ENST00000647125.1:c.121+17C>A ENSP00000496062.1:n.121+17C>A
ENST00000360256.8:c.138C>A ENSP00000353393.4:p.Asp46Glu
ENST00000423959.5:c.38+4365C>A ENSP00000409446.1:n.38+4365C>A
ENST00000453950.1:c.120C>A ENSP00000389153.1:p.Asp40Glu
NM_000132.3:c.138C>A NP_000123.1:p.Asp46Glu
XM_011531126.1:c.38+4365C>A XP_011529428.1:n.38+4365C>A
NM_000132.4:c.138C>A MANE Select NP_000123.1:p.Asp46Glu