Canonical Allele Identifier: CA2466827619

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902051T= , CM000685.2:g.154902051T=	GRCh38
NC_000023.10:g.154130326T= , CM000685.1:g.154130326T=	GRCh37
NC_000023.9:g.153783520T=	NCBI36
NG_011403.1:g.125673A=
NG_011403.2:g.125673A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6115A= MANE Select	ENSP00000353393.4:p.Lys2039=
ENST00000360256.8:c.6115A=	ENSP00000353393.4:p.Lys2039=
NM_000132.3:c.6115A=	NP_000123.1:p.Lys2039=
XM_011531126.1:c.6010A=	XP_011529428.1:p.Lys2004=
NM_000132.4:c.6115A= MANE Select	NP_000123.1:p.Lys2039=