Canonical Allele Identifier: CA2466844438

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154954271C= , CM000685.2:g.154954271C=	GRCh38
NC_000023.10:g.154182546C= , CM000685.1:g.154182546C=	GRCh37
NC_000023.9:g.153835740C=	NCBI36
NG_011403.1:g.73453G=
NG_011403.2:g.73453G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1753-229G= MANE Select	ENSP00000353393.4:n.1753-229G=
ENST00000647125.1:c.*1629-229G=	ENSP00000496062.1:n.*1629-229G=
ENST00000360256.8:c.1753-229G=	ENSP00000353393.4:n.1753-229G=
NM_000132.3:c.1753-229G=	NP_000123.1:n.1753-229G=
XM_011531126.1:c.1648-229G=	XP_011529428.1:n.1648-229G=
NM_000132.4:c.1753-229G= MANE Select	NP_000123.1:n.1753-229G=