Canonical Allele Identifier: CA2466835755

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928650T= , CM000685.2:g.154928650T=	GRCh38
NC_000023.10:g.154156925T= , CM000685.1:g.154156925T=	GRCh37
NC_000023.9:g.153810119T=	NCBI36
NG_011403.1:g.99074A=
NG_011403.2:g.99074A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5140A= MANE Select	ENSP00000353393.4:p.Thr1714=
ENST00000360256.8:c.5140A=	ENSP00000353393.4:p.Thr1714=
NM_000132.3:c.5140A=	NP_000123.1:p.Thr1714=
XM_011531126.1:c.5035A=	XP_011529428.1:p.Thr1679=
NM_000132.4:c.5140A= MANE Select	NP_000123.1:p.Thr1714=