Canonical Allele Identifier: CA2580612537

Gene: F8

Linked Data

• ClinVar Variation Id: 10346
• ClinVar RCV Id: RCV000011059

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904944_154905247delinsA , CM000685.2:g.154904944_154905247delinsA	GRCh38
NC_000023.10:g.154133219_154133522delinsA , CM000685.1:g.154133219_154133522delinsA	GRCh37
NC_000023.9:g.153786413_153786716delinsA	NCBI36
NG_011403.1:g.122477_122780delinsT
NG_011403.2:g.122477_122780delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-224_5453delinsT
ENST00000360256.8:c.5374-224_5453delinsT
NM_000132.3:c.5374-224_5453delinsT
XM_011531126.1:c.5269-224_5348delinsT
NM_000132.4:c.5374-224_5453delinsT