Canonical Allele Identifier: CA2513997001

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905161A>T , CM000685.2:g.154905161A>T	GRCh38
NC_000023.10:g.154133436A>T , CM000685.1:g.154133436A>T	GRCh37
NC_000023.9:g.153786630A>T	NCBI36
NG_011403.1:g.122563T>A
NG_011403.2:g.122563T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-138T>A MANE Select	ENSP00000353393.4:n.5374-138T>A
ENST00000360256.8:c.5374-138T>A	ENSP00000353393.4:n.5374-138T>A
NM_000132.3:c.5374-138T>A	NP_000123.1:n.5374-138T>A
XM_011531126.1:c.5269-138T>A	XP_011529428.1:n.5269-138T>A
NM_000132.4:c.5374-138T>A MANE Select	NP_000123.1:n.5374-138T>A