Canonical Allele Identifier: CA2466848986

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969399G= , CM000685.2:g.154969399G=	GRCh38
NC_000023.10:g.154197674G= , CM000685.1:g.154197674G=	GRCh37
NC_000023.9:g.153850868G=	NCBI36
NG_011403.1:g.58325C=
NG_011403.2:g.58325C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.941C= MANE Select	ENSP00000353393.4:p.Thr314=
ENST00000647125.1:c.*817C=	ENSP00000496062.1:n.*817C=
ENST00000360256.8:c.941C=	ENSP00000353393.4:p.Thr314=
NM_000132.3:c.941C=	NP_000123.1:p.Thr314=
XM_011531126.1:c.836C=	XP_011529428.1:p.Thr279=
NM_000132.4:c.941C= MANE Select	NP_000123.1:p.Thr314=