Canonical Allele Identifier: CA2466827618

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902049A= , CM000685.2:g.154902049A=	GRCh38
NC_000023.10:g.154130324A= , CM000685.1:g.154130324A=	GRCh37
NC_000023.9:g.153783518A=	NCBI36
NG_011403.1:g.125675T=
NG_011403.2:g.125675T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6115+2T= MANE Select	ENSP00000353393.4:n.6115+2T=
ENST00000360256.8:c.6115+2T=	ENSP00000353393.4:n.6115+2T=
NM_000132.3:c.6115+2T=	NP_000123.1:n.6115+2T=
XM_011531126.1:c.6010+2T=	XP_011529428.1:n.6010+2T=
NM_000132.4:c.6115+2T= MANE Select	NP_000123.1:n.6115+2T=