Canonical Allele Identifier: CA2466828149

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903954C= , CM000685.2:g.154903954C=	GRCh38
NC_000023.10:g.154132229C= , CM000685.1:g.154132229C=	GRCh37
NC_000023.9:g.153785423C=	NCBI36
NG_011403.1:g.123770G=
NG_011403.2:g.123770G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5950G= MANE Select	ENSP00000353393.4:p.Val1984=
ENST00000360256.8:c.5950G=	ENSP00000353393.4:p.Val1984=
NM_000132.3:c.5950G=	NP_000123.1:p.Val1984=
XM_011531126.1:c.5845G=	XP_011529428.1:p.Val1949=
NM_000132.4:c.5950G= MANE Select	NP_000123.1:p.Val1984=