Canonical Allele Identifier: CA2695152049
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896249del , CM000685.2:g.154896249del GRCh38
NC_000023.10:g.154124524del , CM000685.1:g.154124524del GRCh37
NC_000023.9:g.153777718del NCBI36
NG_011403.1:g.131475del
NG_011403.2:g.131475del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6274-17del MANE Select ENSP00000353393.4:n.6274-17del
ENST00000360256.8:c.6274-17del ENSP00000353393.4:n.6274-17del
NM_000132.3:c.6274-17del NP_000123.1:n.6274-17del
XM_011531126.1:c.6169-17del XP_011529428.1:n.6169-17del
NM_000132.4:c.6274-17del MANE Select NP_000123.1:n.6274-17del