Canonical Allele Identifier: CA2466827634

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902100G= , CM000685.2:g.154902100G=	GRCh38
NC_000023.10:g.154130375G= , CM000685.1:g.154130375G=	GRCh37
NC_000023.9:g.153783569G=	NCBI36
NG_011403.1:g.125624C=
NG_011403.2:g.125624C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6066C= MANE Select	ENSP00000353393.4:p.Gly2022=
ENST00000360256.8:c.6066C=	ENSP00000353393.4:p.Gly2022=
NM_000132.3:c.6066C=	NP_000123.1:p.Gly2022=
XM_011531126.1:c.5961C=	XP_011529428.1:p.Gly1987=
NM_000132.4:c.6066C= MANE Select	NP_000123.1:p.Gly2022=