Canonical Allele Identifier: CA2466807394

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837561A= , CM000685.2:g.154837561A=	GRCh38
NC_000023.10:g.154065836A= , CM000685.1:g.154065836A=	GRCh37
NC_000023.9:g.153719030A=	NCBI36
NG_011403.1:g.190163T=
NG_033065.1:g.2102T=
NG_011403.2:g.190163T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.*36T= MANE Select	ENSP00000353393.4:n.*36T=
ENST00000644698.1:c.*36T=	ENSP00000495706.1:n.*36T=
ENST00000330287.10:c.*36T=	ENSP00000327895.6:n.*36T=
ENST00000360256.8:c.*36T=	ENSP00000353393.4:n.*36T=
NM_000132.3:c.*36T=	NP_000123.1:n.*36T=
NM_019863.2:c.*36T=	NP_063916.1:n.*36T=
XM_011531126.1:c.*36T=	XP_011529428.1:n.*36T=
NM_000132.4:c.*36T= MANE Select	NP_000123.1:n.*36T=
NM_019863.3:c.*36T=	NP_063916.1:n.*36T=