Canonical Allele Identifier: CA2466845342

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957057T= , CM000685.2:g.154957057T=	GRCh38
NC_000023.10:g.154185332T= , CM000685.1:g.154185332T=	GRCh37
NC_000023.9:g.153838526T=	NCBI36
NG_011403.1:g.70667A=
NG_011403.2:g.70667A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1652A= MANE Select	ENSP00000353393.4:p.Tyr551=
ENST00000647125.1:c.*1528A=	ENSP00000496062.1:n.*1528A=
ENST00000360256.8:c.1652A=	ENSP00000353393.4:p.Tyr551=
NM_000132.3:c.1652A=	NP_000123.1:p.Tyr551=
XM_011531126.1:c.1547A=	XP_011529428.1:p.Tyr516=
NM_000132.4:c.1652A= MANE Select	NP_000123.1:p.Tyr551=