Canonical Allele Identifier: CA2466849041

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969488T= , CM000685.2:g.154969488T=	GRCh38
NC_000023.10:g.154197763T= , CM000685.1:g.154197763T=	GRCh37
NC_000023.9:g.153850957T=	NCBI36
NG_011403.1:g.58236A=
NG_011403.2:g.58236A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.852A= MANE Select	ENSP00000353393.4:p.Glu284=
ENST00000647125.1:c.*728A=	ENSP00000496062.1:n.*728A=
ENST00000360256.8:c.852A=	ENSP00000353393.4:p.Glu284=
NM_000132.3:c.852A=	NP_000123.1:p.Glu284=
XM_011531126.1:c.747A=	XP_011529428.1:p.Glu249=
NM_000132.4:c.852A= MANE Select	NP_000123.1:p.Glu284=