Canonical Allele Identifier: CA2466828457

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904931T= , CM000685.2:g.154904931T=	GRCh38
NC_000023.10:g.154133206T= , CM000685.1:g.154133206T=	GRCh37
NC_000023.9:g.153786400T=	NCBI36
NG_011403.1:g.122793A=
NG_011403.2:g.122793A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5466A= MANE Select	ENSP00000353393.4:p.Arg1822=
ENST00000360256.8:c.5466A=	ENSP00000353393.4:p.Arg1822=
NM_000132.3:c.5466A=	NP_000123.1:p.Arg1822=
XM_011531126.1:c.5361A=	XP_011529428.1:p.Arg1787=
NM_000132.4:c.5466A= MANE Select	NP_000123.1:p.Arg1822=