Canonical Allele Identifier: CA2695237861
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902045_154902057del , CM000685.2:g.154902045_154902057del GRCh38
NC_000023.10:g.154130320_154130332del , CM000685.1:g.154130320_154130332del GRCh37
NC_000023.9:g.153783514_153783526del NCBI36
NG_011403.1:g.125673_125685del
NG_011403.2:g.125673_125685del

Transcript Alleles

HGVS Amino-acid Change
NM_000132.3:c.6115_6115+12del
NM_000132.4:c.6115_6115+12del
ENST00000360256.8:c.6115_6115+12del
ENST00000360256.9:c.6115_6115+12del
XM_011531126.1:c.6010_6010+12del