Canonical Allele Identifier: CA2466849039

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969486A= , CM000685.2:g.154969486A=	GRCh38
NC_000023.10:g.154197761A= , CM000685.1:g.154197761A=	GRCh37
NC_000023.9:g.153850955A=	NCBI36
NG_011403.1:g.58238T=
NG_011403.2:g.58238T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.854T= MANE Select	ENSP00000353393.4:p.Val285=
ENST00000647125.1:c.*730T=	ENSP00000496062.1:n.*730T=
ENST00000360256.8:c.854T=	ENSP00000353393.4:p.Val285=
NM_000132.3:c.854T=	NP_000123.1:p.Val285=
XM_011531126.1:c.749T=	XP_011529428.1:p.Val250=
NM_000132.4:c.854T= MANE Select	NP_000123.1:p.Val285=