Canonical Allele Identifier: CA1969070136

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723356T= , CM000673.2:g.46723356T=	GRCh38
NC_000011.9:g.46744906T= , CM000673.1:g.46744906T=	GRCh37
NC_000011.8:g.46701482T=	NCBI36
NG_008953.1:g.9164T= , LRG_551:g.9164T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.423-26T= MANE Select	ENSP00000308541.5:n.423-26T=
ENST00000311907.9:c.423-26T=	ENSP00000308541.5:n.423-26T=
ENST00000442468.1:c.393-26T=	ENSP00000387413.1:n.393-26T=
ENST00000490274.1:n.177T=
ENST00000530231.5:c.423-26T=	ENSP00000433907.1:n.423-26T=
NM_000506.3:c.423-26T=	NP_000497.1:n.423-26T=
NM_000506.4:c.423-26T= , LRG_551t1:c.423-26T=	NP_000497.1:n.423-26T=
NM_001311257.1:c.375-26T=	NP_001298186.1:n.375-26T=
XR_428840.2:n.467-26T=
XR_428840.4:n.458-26T=
NM_000506.5:c.423-26T= MANE Select	NP_000497.1:n.423-26T=
NM_001311257.2:c.375-26T=	NP_001298186.1:n.375-26T=