Canonical Allele Identifier: CA2466828445

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904897A= , CM000685.2:g.154904897A=	GRCh38
NC_000023.10:g.154133172A= , CM000685.1:g.154133172A=	GRCh37
NC_000023.9:g.153786366A=	NCBI36
NG_011403.1:g.122827T=
NG_011403.2:g.122827T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5500T= MANE Select	ENSP00000353393.4:p.Tyr1834=
ENST00000360256.8:c.5500T=	ENSP00000353393.4:p.Tyr1834=
NM_000132.3:c.5500T=	NP_000123.1:p.Tyr1834=
XM_011531126.1:c.5395T=	XP_011529428.1:p.Tyr1799=
NM_000132.4:c.5500T= MANE Select	NP_000123.1:p.Tyr1834=