Canonical Allele Identifier: CA2466857722

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996849T= , CM000685.2:g.154996849T=	GRCh38
NC_000023.10:g.154225124T= , CM000685.1:g.154225124T=	GRCh37
NC_000023.9:g.153878318T=	NCBI36
NG_011403.1:g.30875A=
NG_011403.2:g.30875A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.388+124A= MANE Select	ENSP00000353393.4:n.388+124A=
ENST00000647125.1:c.*174+124A=	ENSP00000496062.1:n.*174+124A=
ENST00000360256.8:c.388+124A=	ENSP00000353393.4:n.388+124A=
ENST00000423959.5:c.283+124A=	ENSP00000409446.1:n.283+124A=
ENST00000453950.1:c.370+124A=	ENSP00000389153.1:n.370+124A=
NM_000132.3:c.388+124A=	NP_000123.1:n.388+124A=
XM_011531126.1:c.283+124A=	XP_011529428.1:n.283+124A=
NM_000132.4:c.388+124A= MANE Select	NP_000123.1:n.388+124A=