Canonical Allele Identifier: CA2695237160
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863080_154863083del , CM000685.2:g.154863080_154863083del GRCh38
NC_000023.10:g.154091355_154091358del , CM000685.1:g.154091355_154091358del GRCh37
NC_000023.9:g.153744549_153744552del NCBI36
NG_011403.1:g.164644_164647del
NG_011403.2:g.164644_164647del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6574+3_6574+6del
ENST00000644698.1:c.307+3_307+6del
ENST00000330287.10:c.169+3_169+6del
ENST00000360256.8:c.6574+3_6574+6del
NM_000132.3:c.6574+3_6574+6del
NM_019863.2:c.169+3_169+6del
XM_011531126.1:c.6469+3_6469+6del
NM_000132.4:c.6574+3_6574+6del
NM_019863.3:c.169+3_169+6del