Canonical Allele Identifier: CA2695168202
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905095del , CM000685.2:g.154905095del GRCh38
NC_000023.10:g.154133370del , CM000685.1:g.154133370del GRCh37
NC_000023.9:g.153786564del NCBI36
NG_011403.1:g.122629del
NG_011403.2:g.122629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5374-72del MANE Select ENSP00000353393.4:n.5374-72del
ENST00000360256.8:c.5374-72del ENSP00000353393.4:n.5374-72del
NM_000132.3:c.5374-72del NP_000123.1:n.5374-72del
XM_011531126.1:c.5269-72del XP_011529428.1:n.5269-72del
NM_000132.4:c.5374-72del MANE Select NP_000123.1:n.5374-72del