Canonical Allele Identifier: CA5967314

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46729406G>A , CM000673.2:g.46729406G>A	GRCh38
NC_000011.9:g.46750956G>A , CM000673.1:g.46750956G>A	GRCh37
NC_000011.8:g.46707532G>A	NCBI36
NG_008953.1:g.15214G>A , LRG_551:g.15214G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000506.5:c.1499G>A MANE Select	NP_000497.1:p.Arg500Gln
ENST00000311907.10:c.1499G>A MANE Select	ENSP00000308541.5:p.Arg500Gln
NM_000506.3:c.1499G>A	NP_000497.1:p.Arg500Gln
NM_000506.4:c.1499G>A , LRG_551t1:c.1499G>A	NP_000497.1:p.Arg500Gln
NM_001311257.1:c.1451G>A	NP_001298186.1:p.Arg484Gln
NM_001311257.2:c.1451G>A	NP_001298186.1:p.Arg484Gln
ENST00000311907.9:c.1499G>A	ENSP00000308541.5:p.Arg500Gln
ENST00000530231.5:c.1382G>A	ENSP00000433907.1:p.Arg461Gln
XR_428840.2:n.1516+569G>A
XR_428840.4:n.1507+569G>A