Canonical Allele Identifier: CA2695152055
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896259del , CM000685.2:g.154896259del GRCh38
NC_000023.10:g.154124534del , CM000685.1:g.154124534del GRCh37
NC_000023.9:g.153777728del NCBI36
NG_011403.1:g.131468del
NG_011403.2:g.131468del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6274-24del MANE Select ENSP00000353393.4:n.6274-24del
ENST00000360256.8:c.6274-24del ENSP00000353393.4:n.6274-24del
NM_000132.3:c.6274-24del NP_000123.1:n.6274-24del
XM_011531126.1:c.6169-24del XP_011529428.1:n.6169-24del
NM_000132.4:c.6274-24del MANE Select NP_000123.1:n.6274-24del