Canonical Allele Identifier: CA2466857721

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996847T= , CM000685.2:g.154996847T=	GRCh38
NC_000023.10:g.154225122T= , CM000685.1:g.154225122T=	GRCh37
NC_000023.9:g.153878316T=	NCBI36
NG_011403.1:g.30877A=
NG_011403.2:g.30877A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.388+126A= MANE Select	ENSP00000353393.4:n.388+126A=
ENST00000647125.1:c.*174+126A=	ENSP00000496062.1:n.*174+126A=
ENST00000360256.8:c.388+126A=	ENSP00000353393.4:n.388+126A=
ENST00000423959.5:c.283+126A=	ENSP00000409446.1:n.283+126A=
ENST00000453950.1:c.370+126A=	ENSP00000389153.1:n.370+126A=
NM_000132.3:c.388+126A=	NP_000123.1:n.388+126A=
XM_011531126.1:c.283+126A=	XP_011529428.1:n.283+126A=
NM_000132.4:c.388+126A= MANE Select	NP_000123.1:n.388+126A=