Canonical Allele Identifier: CA2695237268

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957164_154957182del , CM000685.2:g.154957164_154957182del	GRCh38
NC_000023.10:g.154185439_154185457del , CM000685.1:g.154185439_154185457del	GRCh37
NC_000023.9:g.153838633_153838651del	NCBI36
NG_011403.1:g.70543_70561del
NG_011403.2:g.70543_70561del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1538-10_1546del
ENST00000647125.1:c.*1414-10_*1422del
ENST00000360256.8:c.1538-10_1546del
NM_000132.3:c.1538-10_1546del
XM_011531126.1:c.1433-10_1441del
NM_000132.4:c.1538-10_1546del