Canonical Allele Identifier: CA2466828130

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903911T= , CM000685.2:g.154903911T=	GRCh38
NC_000023.10:g.154132186T= , CM000685.1:g.154132186T=	GRCh37
NC_000023.9:g.153785380T=	NCBI36
NG_011403.1:g.123813A=
NG_011403.2:g.123813A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.5993A= MANE Select	ENSP00000353393.4:p.Tyr1998=
ENST00000360256.8:c.5993A=	ENSP00000353393.4:p.Tyr1998=
NM_000132.3:c.5993A=	NP_000123.1:p.Tyr1998=
XM_011531126.1:c.5888A=	XP_011529428.1:p.Tyr1963=
NM_000132.4:c.5993A= MANE Select	NP_000123.1:p.Tyr1998=