Canonical Allele Identifier: CA2466815007

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860529T= , CM000685.2:g.154860529T=	GRCh38
NC_000023.10:g.154088804T= , CM000685.1:g.154088804T=	GRCh37
NC_000023.9:g.153741998T=	NCBI36
NG_011403.1:g.167195A=
NG_011403.2:g.167195A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6803A= MANE Select	ENSP00000353393.4:p.Lys2268=
ENST00000644698.1:c.536A=	ENSP00000495706.1:p.Lys179=
ENST00000330287.10:c.398A=	ENSP00000327895.6:p.Lys133=
ENST00000360256.8:c.6803A=	ENSP00000353393.4:p.Lys2268=
NM_000132.3:c.6803A=	NP_000123.1:p.Lys2268=
NM_019863.2:c.398A=	NP_063916.1:p.Lys133=
XM_011531126.1:c.6698A=	XP_011529428.1:p.Lys2233=
NM_000132.4:c.6803A= MANE Select	NP_000123.1:p.Lys2268=
NM_019863.3:c.398A=	NP_063916.1:p.Lys133=