Canonical Allele Identifier: CA2695237903

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902167_154902189del , CM000685.2:g.154902167_154902189del	GRCh38
NC_000023.10:g.154130442_154130464del , CM000685.1:g.154130442_154130464del	GRCh37
NC_000023.9:g.153783636_153783658del	NCBI36
NG_011403.1:g.125539_125561del
NG_011403.2:g.125539_125561del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5999-18_6003del
ENST00000360256.8:c.5999-18_6003del
NM_000132.3:c.5999-18_6003del
XM_011531126.1:c.5894-18_5898del
NM_000132.4:c.5999-18_6003del