Canonical Allele Identifier: CA2466865514

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022720A= , CM000685.2:g.155022720A=	GRCh38
NC_000023.10:g.154250995A= , CM000685.1:g.154250995A=	GRCh37
NC_000023.9:g.153904189A=	NCBI36
NG_011403.1:g.5004T=
NG_011403.2:g.5004T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-168T= MANE Select	ENSP00000353393.4:n.-168T=
ENST00000360256.8:c.-168T=	ENSP00000353393.4:n.-168T=
ENST00000423959.5:c.38+4060T=	ENSP00000409446.1:n.38+4060T=
ENST00000453950.1:c.39-224T=	ENSP00000389153.1:n.39-224T=
NM_000132.3:c.-168T=	NP_000123.1:n.-168T=
XM_011531126.1:c.38+4060T=	XP_011529428.1:n.38+4060T=
NM_000132.4:c.-168T= MANE Select	NP_000123.1:n.-168T=