Canonical Allele Identifier: CA2466807418

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837617C= , CM000685.2:g.154837617C=	GRCh38
NC_000023.10:g.154065892C= , CM000685.1:g.154065892C=	GRCh37
NC_000023.9:g.153719086C=	NCBI36
NG_011403.1:g.190107G=
NG_033065.1:g.2046G=
NG_011403.2:g.190107G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.7036G= MANE Select	ENSP00000353393.4:p.Glu2346=
ENST00000644698.1:c.769G=	ENSP00000495706.1:p.Glu257=
ENST00000330287.10:c.631G=	ENSP00000327895.6:p.Glu211=
ENST00000360256.8:c.7036G=	ENSP00000353393.4:p.Glu2346=
NM_000132.3:c.7036G=	NP_000123.1:p.Glu2346=
NM_019863.2:c.631G=	NP_063916.1:p.Glu211=
XM_011531126.1:c.6931G=	XP_011529428.1:p.Glu2311=
NM_000132.4:c.7036G= MANE Select	NP_000123.1:p.Glu2346=
NM_019863.3:c.631G=	NP_063916.1:p.Glu211=