Canonical Allele Identifier: CA2466849038

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969485C= , CM000685.2:g.154969485C=	GRCh38
NC_000023.10:g.154197760C= , CM000685.1:g.154197760C=	GRCh37
NC_000023.9:g.153850954C=	NCBI36
NG_011403.1:g.58239G=
NG_011403.2:g.58239G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.855G= MANE Select	ENSP00000353393.4:p.Val285=
ENST00000647125.1:c.*731G=	ENSP00000496062.1:n.*731G=
ENST00000360256.8:c.855G=	ENSP00000353393.4:p.Val285=
NM_000132.3:c.855G=	NP_000123.1:p.Val285=
XM_011531126.1:c.750G=	XP_011529428.1:p.Val250=
NM_000132.4:c.855G= MANE Select	NP_000123.1:p.Val285=