Canonical Allele Identifier: CA414911860
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957068G>T , CM000685.2:g.154957068G>T GRCh38
NC_000023.10:g.154185343G>T , CM000685.1:g.154185343G>T GRCh37
NC_000023.9:g.153838537G>T NCBI36
NG_011403.1:g.70656C>A
NG_011403.2:g.70656C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1641C>A MANE Select ENSP00000353393.4:p.Cys547Ter
ENST00000647125.1:c.*1517C>A ENSP00000496062.1:n.*1517C>A
ENST00000360256.8:c.1641C>A ENSP00000353393.4:p.Cys547Ter
NM_000132.3:c.1641C>A NP_000123.1:p.Cys547Ter
XM_011531126.1:c.1536C>A XP_011529428.1:p.Cys512Ter
NM_000132.4:c.1641C>A MANE Select NP_000123.1:p.Cys547Ter