Canonical Allele Identifier: CA873340070
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1397860873

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928592dup , CM000685.2:g.154928592dup GRCh38
NC_000023.10:g.154156867dup , CM000685.1:g.154156867dup GRCh37
NC_000023.9:g.153810061dup NCBI36
NG_011403.1:g.99135dup
NG_011403.2:g.99135dup

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5201dup MANE Select ENSP00000353393.4:p.His1735ThrfsTer25
ENST00000360256.8:c.5201dup ENSP00000353393.4:p.His1735ThrfsTer25
NM_000132.3:c.5201dup NP_000123.1:p.His1735ThrfsTer25
XM_011531126.1:c.5096dup XP_011529428.1:p.His1700ThrfsTer25
NM_000132.4:c.5201dup MANE Select NP_000123.1:p.His1735ThrfsTer25