Canonical Allele Identifier: CA2466828437

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904883C= , CM000685.2:g.154904883C=	GRCh38
NC_000023.10:g.154133158C= , CM000685.1:g.154133158C=	GRCh37
NC_000023.9:g.153786352C=	NCBI36
NG_011403.1:g.122841G=
NG_011403.2:g.122841G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5514G= MANE Select	ENSP00000353393.4:p.Val1838=
ENST00000360256.8:c.5514G=	ENSP00000353393.4:p.Val1838=
NM_000132.3:c.5514G=	NP_000123.1:p.Val1838=
XM_011531126.1:c.5409G=	XP_011529428.1:p.Val1803=
NM_000132.4:c.5514G= MANE Select	NP_000123.1:p.Val1838=