Canonical Allele Identifier: CA1969070187

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723381G= , CM000673.2:g.46723381G=	GRCh38
NC_000011.9:g.46744931G= , CM000673.1:g.46744931G=	GRCh37
NC_000011.8:g.46701507G=	NCBI36
NG_008953.1:g.9189G= , LRG_551:g.9189G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.423-1G= MANE Select	ENSP00000308541.5:n.423-1G=
ENST00000311907.9:c.423-1G=	ENSP00000308541.5:n.423-1G=
ENST00000442468.1:c.393-1G=	ENSP00000387413.1:n.393-1G=
ENST00000490274.1:n.202G=
ENST00000530231.5:c.423-1G=	ENSP00000433907.1:n.423-1G=
NM_000506.3:c.423-1G=	NP_000497.1:n.423-1G=
NM_000506.4:c.423-1G= , LRG_551t1:c.423-1G=	NP_000497.1:n.423-1G=
NM_001311257.1:c.375-1G=	NP_001298186.1:n.375-1G=
XR_428840.2:n.467-1G=
XR_428840.4:n.458-1G=
NM_000506.5:c.423-1G= MANE Select	NP_000497.1:n.423-1G=
NM_001311257.2:c.375-1G=	NP_001298186.1:n.375-1G=