Canonical Allele Identifier: CA2466828439

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904890C= , CM000685.2:g.154904890C=	GRCh38
NC_000023.10:g.154133165C= , CM000685.1:g.154133165C=	GRCh37
NC_000023.9:g.153786359C=	NCBI36
NG_011403.1:g.122834G=
NG_011403.2:g.122834G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5507G= MANE Select	ENSP00000353393.4:p.Trp1836=
ENST00000360256.8:c.5507G=	ENSP00000353393.4:p.Trp1836=
NM_000132.3:c.5507G=	NP_000123.1:p.Trp1836=
XM_011531126.1:c.5402G=	XP_011529428.1:p.Trp1801=
NM_000132.4:c.5507G= MANE Select	NP_000123.1:p.Trp1836=