Canonical Allele Identifier: CA2466807422

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837623C= , CM000685.2:g.154837623C=	GRCh38
NC_000023.10:g.154065898C= , CM000685.1:g.154065898C=	GRCh37
NC_000023.9:g.153719092C=	NCBI36
NG_011403.1:g.190101G=
NG_033065.1:g.2040G=
NG_011403.2:g.190101G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7030G= MANE Select	ENSP00000353393.4:p.Gly2344=
ENST00000644698.1:c.763G=	ENSP00000495706.1:p.Gly255=
ENST00000330287.10:c.625G=	ENSP00000327895.6:p.Gly209=
ENST00000360256.8:c.7030G=	ENSP00000353393.4:p.Gly2344=
NM_000132.3:c.7030G=	NP_000123.1:p.Gly2344=
NM_019863.2:c.625G=	NP_063916.1:p.Gly209=
XM_011531126.1:c.6925G=	XP_011529428.1:p.Gly2309=
NM_000132.4:c.7030G= MANE Select	NP_000123.1:p.Gly2344=
NM_019863.3:c.625G=	NP_063916.1:p.Gly209=