Canonical Allele Identifier: CA2466815651

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863152G= , CM000685.2:g.154863152G=	GRCh38
NC_000023.10:g.154091427G= , CM000685.1:g.154091427G=	GRCh37
NC_000023.9:g.153744621G=	NCBI36
NG_011403.1:g.164572C=
NG_011403.2:g.164572C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6505C= MANE Select	ENSP00000353393.4:p.Arg2169=
ENST00000644698.1:c.238C=	ENSP00000495706.1:p.Arg80=
ENST00000330287.10:c.100C=	ENSP00000327895.6:p.Arg34=
ENST00000360256.8:c.6505C=	ENSP00000353393.4:p.Arg2169=
NM_000132.3:c.6505C=	NP_000123.1:p.Arg2169=
NM_019863.2:c.100C=	NP_063916.1:p.Arg34=
XM_011531126.1:c.6400C=	XP_011529428.1:p.Arg2134=
NM_000132.4:c.6505C= MANE Select	NP_000123.1:p.Arg2169=
NM_019863.3:c.100C=	NP_063916.1:p.Arg34=