Canonical Allele Identifier: CA5966990

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723523G>A , CM000673.2:g.46723523G>A	GRCh38
NC_000011.9:g.46745073G>A , CM000673.1:g.46745073G>A	GRCh37
NC_000011.8:g.46701649G>A	NCBI36
NG_008953.1:g.9331G>A , LRG_551:g.9331G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.559+5G>A MANE Select	ENSP00000308541.5:n.559+5G>A
ENST00000311907.9:c.559+5G>A	ENSP00000308541.5:n.559+5G>A
ENST00000442468.1:c.529+5G>A	ENSP00000387413.1:n.529+5G>A
ENST00000490274.1:n.339+5G>A
ENST00000530231.5:c.559+5G>A	ENSP00000433907.1:n.559+5G>A
NM_000506.3:c.559+5G>A	NP_000497.1:n.559+5G>A
NM_000506.4:c.559+5G>A , LRG_551t1:c.559+5G>A	NP_000497.1:n.559+5G>A
NM_001311257.1:c.511+5G>A	NP_001298186.1:n.511+5G>A
XR_428840.2:n.603+5G>A
XR_428840.4:n.594+5G>A
NM_000506.5:c.559+5G>A MANE Select	NP_000497.1:n.559+5G>A
NM_001311257.2:c.511+5G>A	NP_001298186.1:n.511+5G>A