Canonical Allele Identifier: CA2466856587

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993187A= , CM000685.2:g.154993187A=	GRCh38
NC_000023.10:g.154221462A= , CM000685.1:g.154221462A=	GRCh37
NC_000023.9:g.153874656A=	NCBI36
NG_011403.1:g.34537T=
NG_011403.2:g.34537T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.389-39T= MANE Select	ENSP00000353393.4:n.389-39T=
ENST00000647125.1:c.*175-39T=	ENSP00000496062.1:n.*175-39T=
ENST00000360256.8:c.389-39T=	ENSP00000353393.4:n.389-39T=
ENST00000423959.5:c.284-39T=	ENSP00000409446.1:n.284-39T=
ENST00000453950.1:c.371-39T=	ENSP00000389153.1:n.371-39T=
NM_000132.3:c.389-39T=	NP_000123.1:n.389-39T=
XM_011531126.1:c.284-39T=	XP_011529428.1:n.284-39T=
NM_000132.4:c.389-39T= MANE Select	NP_000123.1:n.389-39T=