Canonical Allele Identifier: CA2466848168

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154966671A= , CM000685.2:g.154966671A=	GRCh38
NC_000023.10:g.154194946A= , CM000685.1:g.154194946A=	GRCh37
NC_000023.9:g.153848140A=	NCBI36
NG_011403.1:g.61053T=
NG_011403.2:g.61053T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1026T= MANE Select	ENSP00000353393.4:p.Tyr342=
ENST00000647125.1:c.*902T=	ENSP00000496062.1:n.*902T=
ENST00000360256.8:c.1026T=	ENSP00000353393.4:p.Tyr342=
NM_000132.3:c.1026T=	NP_000123.1:p.Tyr342=
XM_011531126.1:c.921T=	XP_011529428.1:p.Tyr307=
NM_000132.4:c.1026T= MANE Select	NP_000123.1:p.Tyr342=