Canonical Allele Identifier: CA2466807467

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837742C= , CM000685.2:g.154837742C=	GRCh38
NC_000023.10:g.154066017C= , CM000685.1:g.154066017C=	GRCh37
NC_000023.9:g.153719211C=	NCBI36
NG_011403.1:g.189982G=
NG_033065.1:g.1921G=
NG_011403.2:g.189982G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6911G= MANE Select	ENSP00000353393.4:p.Gly2304=
ENST00000644698.1:c.644G=	ENSP00000495706.1:p.Gly215=
ENST00000330287.10:c.506G=	ENSP00000327895.6:p.Gly169=
ENST00000360256.8:c.6911G=	ENSP00000353393.4:p.Gly2304=
NM_000132.3:c.6911G=	NP_000123.1:p.Gly2304=
NM_019863.2:c.506G=	NP_063916.1:p.Gly169=
XM_011531126.1:c.6806G=	XP_011529428.1:p.Gly2269=
NM_000132.4:c.6911G= MANE Select	NP_000123.1:p.Gly2304=
NM_019863.3:c.506G=	NP_063916.1:p.Gly169=