Canonical Allele Identifier: CA2466856578

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993152T= , CM000685.2:g.154993152T=	GRCh38
NC_000023.10:g.154221427T= , CM000685.1:g.154221427T=	GRCh37
NC_000023.9:g.153874621T=	NCBI36
NG_011403.1:g.34572A=
NG_011403.2:g.34572A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.389-4A= MANE Select	ENSP00000353393.4:n.389-4A=
ENST00000647125.1:c.*175-4A=	ENSP00000496062.1:n.*175-4A=
ENST00000360256.8:c.389-4A=	ENSP00000353393.4:n.389-4A=
ENST00000423959.5:c.284-4A=	ENSP00000409446.1:n.284-4A=
ENST00000453950.1:c.371-4A=	ENSP00000389153.1:n.371-4A=
NM_000132.3:c.389-4A=	NP_000123.1:n.389-4A=
XM_011531126.1:c.284-4A=	XP_011529428.1:n.284-4A=
NM_000132.4:c.389-4A= MANE Select	NP_000123.1:n.389-4A=