Canonical Allele Identifier: CA2466857720

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996839C= , CM000685.2:g.154996839C=	GRCh38
NC_000023.10:g.154225114C= , CM000685.1:g.154225114C=	GRCh37
NC_000023.9:g.153878308C=	NCBI36
NG_011403.1:g.30885G=
NG_011403.2:g.30885G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.388+134G= MANE Select	ENSP00000353393.4:n.388+134G=
ENST00000647125.1:c.*174+134G=	ENSP00000496062.1:n.*174+134G=
ENST00000360256.8:c.388+134G=	ENSP00000353393.4:n.388+134G=
ENST00000423959.5:c.283+134G=	ENSP00000409446.1:n.283+134G=
ENST00000453950.1:c.370+134G=	ENSP00000389153.1:n.370+134G=
NM_000132.3:c.388+134G=	NP_000123.1:n.388+134G=
XM_011531126.1:c.283+134G=	XP_011529428.1:n.283+134G=
NM_000132.4:c.388+134G= MANE Select	NP_000123.1:n.388+134G=