Canonical Allele Identifier: CA2466856705

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993534G= , CM000685.2:g.154993534G=	GRCh38
NC_000023.10:g.154221809G= , CM000685.1:g.154221809G=	GRCh37
NC_000023.9:g.153875003G=	NCBI36
NG_011403.1:g.34190C=
NG_011403.2:g.34190C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.389-386C= MANE Select	ENSP00000353393.4:n.389-386C=
ENST00000647125.1:c.*175-386C=	ENSP00000496062.1:n.*175-386C=
ENST00000360256.8:c.389-386C=	ENSP00000353393.4:n.389-386C=
ENST00000423959.5:c.284-386C=	ENSP00000409446.1:n.284-386C=
ENST00000453950.1:c.371-386C=	ENSP00000389153.1:n.371-386C=
NM_000132.3:c.389-386C=	NP_000123.1:n.389-386C=
XM_011531126.1:c.284-386C=	XP_011529428.1:n.284-386C=
NM_000132.4:c.389-386C= MANE Select	NP_000123.1:n.389-386C=