Canonical Allele Identifier: CA2466848984

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969388G= , CM000685.2:g.154969388G=	GRCh38
NC_000023.10:g.154197663G= , CM000685.1:g.154197663G=	GRCh37
NC_000023.9:g.153850857G=	NCBI36
NG_011403.1:g.58336C=
NG_011403.2:g.58336C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.952C= MANE Select	ENSP00000353393.4:p.Leu318=
ENST00000647125.1:c.*828C=	ENSP00000496062.1:n.*828C=
ENST00000360256.8:c.952C=	ENSP00000353393.4:p.Leu318=
NM_000132.3:c.952C=	NP_000123.1:p.Leu318=
XM_011531126.1:c.847C=	XP_011529428.1:p.Leu283=
NM_000132.4:c.952C= MANE Select	NP_000123.1:p.Leu318=