Canonical Allele Identifier: CA414909059
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905002A>T , CM000685.2:g.154905002A>T GRCh38
NC_000023.10:g.154133277A>T , CM000685.1:g.154133277A>T GRCh37
NC_000023.9:g.153786471A>T NCBI36
NG_011403.1:g.122722T>A
NG_011403.2:g.122722T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5395T>A MANE Select ENSP00000353393.4:p.Ser1799Thr
ENST00000360256.8:c.5395T>A ENSP00000353393.4:p.Ser1799Thr
NM_000132.3:c.5395T>A NP_000123.1:p.Ser1799Thr
XM_011531126.1:c.5290T>A XP_011529428.1:p.Ser1764Thr
NM_000132.4:c.5395T>A MANE Select NP_000123.1:p.Ser1799Thr