Canonical Allele Identifier: CA2695237407
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969329_154969448del , CM000685.2:g.154969329_154969448del GRCh38
NC_000023.10:g.154197604_154197723del , CM000685.1:g.154197604_154197723del GRCh37
NC_000023.9:g.153850798_153850917del NCBI36
NG_011403.1:g.58277_58396del
NG_011403.2:g.58277_58396del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.893_1009+3del
ENST00000647125.1:c.*769_*885+3del
ENST00000360256.8:c.893_1009+3del
NM_000132.3:c.893_1009+3del
XM_011531126.1:c.788_904+3del
NM_000132.4:c.893_1009+3del