Canonical Allele Identifier: CA2466848983

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969385A= , CM000685.2:g.154969385A=	GRCh38
NC_000023.10:g.154197660A= , CM000685.1:g.154197660A=	GRCh37
NC_000023.9:g.153850854A=	NCBI36
NG_011403.1:g.58339T=
NG_011403.2:g.58339T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.955T= MANE Select	ENSP00000353393.4:p.Leu319=
ENST00000647125.1:c.*831T=	ENSP00000496062.1:n.*831T=
ENST00000360256.8:c.955T=	ENSP00000353393.4:p.Leu319=
NM_000132.3:c.955T=	NP_000123.1:p.Leu319=
XM_011531126.1:c.850T=	XP_011529428.1:p.Leu284=
NM_000132.4:c.955T= MANE Select	NP_000123.1:p.Leu319=