Canonical Allele Identifier: CA2466836658

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154931348T= , CM000685.2:g.154931348T=	GRCh38
NC_000023.10:g.154159623T= , CM000685.1:g.154159623T=	GRCh37
NC_000023.9:g.153812817T=	NCBI36
NG_011403.1:g.96376A=
NG_011403.2:g.96376A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.2442A= MANE Select	ENSP00000353393.4:p.Arg814=
ENST00000647125.1:c.*2108A=	ENSP00000496062.1:n.*2108A=
ENST00000360256.8:c.2442A=	ENSP00000353393.4:p.Arg814=
NM_000132.3:c.2442A=	NP_000123.1:p.Arg814=
XM_011531126.1:c.2337A=	XP_011529428.1:p.Arg779=
NM_000132.4:c.2442A= MANE Select	NP_000123.1:p.Arg814=