Canonical Allele Identifier: CA1969071914

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725875T= , CM000673.2:g.46725875T=	GRCh38
NC_000011.9:g.46747425T= , CM000673.1:g.46747425T=	GRCh37
NC_000011.8:g.46704001T=	NCBI36
NG_008953.1:g.11683T= , LRG_551:g.11683T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.576T= MANE Select	ENSP00000308541.5:p.Thr192=
ENST00000311907.9:c.576T=	ENSP00000308541.5:p.Thr192=
ENST00000442468.1:c.546T=	ENSP00000387413.1:p.Thr182=
ENST00000490274.1:n.356T=
ENST00000530231.5:c.576T=	ENSP00000433907.1:p.Thr192=
NM_000506.3:c.576T=	NP_000497.1:p.Thr192=
NM_000506.4:c.576T= , LRG_551t1:c.576T=	NP_000497.1:p.Thr192=
NM_001311257.1:c.528T=	NP_001298186.1:p.Thr176=
XR_428840.2:n.620T=
XR_428840.4:n.611T=
NM_000506.5:c.576T= MANE Select	NP_000497.1:p.Thr192=
NM_001311257.2:c.528T=	NP_001298186.1:p.Thr176=