Canonical Allele Identifier: CA2466828372

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904684A= , CM000685.2:g.154904684A=	GRCh38
NC_000023.10:g.154132959A= , CM000685.1:g.154132959A=	GRCh37
NC_000023.9:g.153786153A=	NCBI36
NG_011403.1:g.123040T=
NG_011403.2:g.123040T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5586+127T= MANE Select	ENSP00000353393.4:n.5586+127T=
ENST00000360256.8:c.5586+127T=	ENSP00000353393.4:n.5586+127T=
NM_000132.3:c.5586+127T=	NP_000123.1:n.5586+127T=
XM_011531126.1:c.5481+127T=	XP_011529428.1:n.5481+127T=
NM_000132.4:c.5586+127T= MANE Select	NP_000123.1:n.5586+127T=