Canonical Allele Identifier: CA2466848102

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154966466C= , CM000685.2:g.154966466C=	GRCh38
NC_000023.10:g.154194741C= , CM000685.1:g.154194741C=	GRCh37
NC_000023.9:g.153847935C=	NCBI36
NG_011403.1:g.61258G=
NG_011403.2:g.61258G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1231G= MANE Select	ENSP00000353393.4:p.Asp411=
ENST00000647125.1:c.*1107G=	ENSP00000496062.1:n.*1107G=
ENST00000360256.8:c.1231G=	ENSP00000353393.4:p.Asp411=
ENST00000483822.2:n.51G=
NM_000132.3:c.1231G=	NP_000123.1:p.Asp411=
XM_011531126.1:c.1126G=	XP_011529428.1:p.Asp376=
NM_000132.4:c.1231G= MANE Select	NP_000123.1:p.Asp411=