Canonical Allele Identifier: CA2466807342

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837434C= , CM000685.2:g.154837434C=	GRCh38
NC_000023.10:g.154065709C= , CM000685.1:g.154065709C=	GRCh37
NC_000023.9:g.153718903C=	NCBI36
NG_011403.1:g.190290G=
NG_033065.1:g.2229G=
NG_011403.2:g.190290G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.*163G= MANE Select	ENSP00000353393.4:n.*163G=
ENST00000644698.1:c.*163G=	ENSP00000495706.1:n.*163G=
ENST00000330287.10:c.*163G=	ENSP00000327895.6:n.*163G=
ENST00000360256.8:c.*163G=	ENSP00000353393.4:n.*163G=
NM_000132.3:c.*163G=	NP_000123.1:n.*163G=
NM_019863.2:c.*163G=	NP_063916.1:n.*163G=
XM_011531126.1:c.*163G=	XP_011529428.1:n.*163G=
NM_000132.4:c.*163G= MANE Select	NP_000123.1:n.*163G=
NM_019863.3:c.*163G=	NP_063916.1:n.*163G=