Canonical Allele Identifier: CA2466828211

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904122T= , CM000685.2:g.154904122T=	GRCh38
NC_000023.10:g.154132397T= , CM000685.1:g.154132397T=	GRCh37
NC_000023.9:g.153785591T=	NCBI36
NG_011403.1:g.123602A=
NG_011403.2:g.123602A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5816-34A= MANE Select	ENSP00000353393.4:n.5816-34A=
ENST00000360256.8:c.5816-34A=	ENSP00000353393.4:n.5816-34A=
NM_000132.3:c.5816-34A=	NP_000123.1:n.5816-34A=
XM_011531126.1:c.5711-34A=	XP_011529428.1:n.5711-34A=
NM_000132.4:c.5816-34A= MANE Select	NP_000123.1:n.5816-34A=