Canonical Allele Identifier: CA2466836692

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154931449G= , CM000685.2:g.154931449G=	GRCh38
NC_000023.10:g.154159724G= , CM000685.1:g.154159724G=	GRCh37
NC_000023.9:g.153812918G=	NCBI36
NG_011403.1:g.96275C=
NG_011403.2:g.96275C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.2341C= MANE Select	ENSP00000353393.4:p.Pro781=
ENST00000647125.1:c.*2007C=	ENSP00000496062.1:n.*2007C=
ENST00000360256.8:c.2341C=	ENSP00000353393.4:p.Pro781=
NM_000132.3:c.2341C=	NP_000123.1:p.Pro781=
XM_011531126.1:c.2236C=	XP_011529428.1:p.Pro746=
NM_000132.4:c.2341C= MANE Select	NP_000123.1:p.Pro781=