Canonical Allele Identifier: CA2466842536

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154947767C= , CM000685.2:g.154947767C=	GRCh38
NC_000023.10:g.154176042C= , CM000685.1:g.154176042C=	GRCh37
NC_000023.9:g.153829236C=	NCBI36
NG_011403.1:g.79957G=
NG_011403.2:g.79957G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.2044G= MANE Select	ENSP00000353393.4:p.Val682=
ENST00000647125.1:c.*1779+6125G=	ENSP00000496062.1:n.*1779+6125G=
ENST00000360256.8:c.2044G=	ENSP00000353393.4:p.Val682=
NM_000132.3:c.2044G=	NP_000123.1:p.Val682=
XM_011531126.1:c.1939G=	XP_011529428.1:p.Val647=
NM_000132.4:c.2044G= MANE Select	NP_000123.1:p.Val682=