Canonical Allele Identifier: CA3008791289
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997096dup , CM000685.2:g.154997096dup GRCh38
NC_000023.10:g.154225371dup , CM000685.1:g.154225371dup GRCh37
NC_000023.9:g.153878565dup NCBI36
NG_011403.1:g.30629dup
NG_011403.2:g.30629dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.266dup
ENST00000647125.1:c.*52dup
ENST00000360256.8:c.266dup
ENST00000423959.5:c.161dup
ENST00000453950.1:c.248dup
NM_000132.3:c.266dup
XM_011531126.1:c.161dup
NM_000132.4:c.266dup