Canonical Allele Identifier: CA2466828118

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903870G= , CM000685.2:g.154903870G=	GRCh38
NC_000023.10:g.154132145G= , CM000685.1:g.154132145G=	GRCh37
NC_000023.9:g.153785339G=	NCBI36
NG_011403.1:g.123854C=
NG_011403.2:g.123854C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5998+36C= MANE Select	ENSP00000353393.4:n.5998+36C=
ENST00000360256.8:c.5998+36C=	ENSP00000353393.4:n.5998+36C=
NM_000132.3:c.5998+36C=	NP_000123.1:n.5998+36C=
XM_011531126.1:c.5893+36C=	XP_011529428.1:n.5893+36C=
NM_000132.4:c.5998+36C= MANE Select	NP_000123.1:n.5998+36C=