Canonical Allele Identifier: CA2466844469

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154954369T= , CM000685.2:g.154954369T=	GRCh38
NC_000023.10:g.154182644T= , CM000685.1:g.154182644T=	GRCh37
NC_000023.9:g.153835838T=	NCBI36
NG_011403.1:g.73355A=
NG_011403.2:g.73355A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1753-327A= MANE Select	ENSP00000353393.4:n.1753-327A=
ENST00000647125.1:c.*1629-327A=	ENSP00000496062.1:n.*1629-327A=
ENST00000360256.8:c.1753-327A=	ENSP00000353393.4:n.1753-327A=
NM_000132.3:c.1753-327A=	NP_000123.1:n.1753-327A=
XM_011531126.1:c.1648-327A=	XP_011529428.1:n.1648-327A=
NM_000132.4:c.1753-327A= MANE Select	NP_000123.1:n.1753-327A=