Canonical Allele Identifier: CA5967318

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46729448A>G , CM000673.2:g.46729448A>G	GRCh38
NC_000011.9:g.46750998A>G , CM000673.1:g.46750998A>G	GRCh37
NC_000011.8:g.46707574A>G	NCBI36
NG_008953.1:g.15256A>G , LRG_551:g.15256A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1541A>G MANE Select	ENSP00000308541.5:p.Asn514Ser
ENST00000311907.9:c.1541A>G	ENSP00000308541.5:p.Asn514Ser
ENST00000530231.5:c.1424A>G	ENSP00000433907.1:p.Asn475Ser
NM_000506.3:c.1541A>G	NP_000497.1:p.Asn514Ser
NM_000506.4:c.1541A>G , LRG_551t1:c.1541A>G	NP_000497.1:p.Asn514Ser
NM_001311257.1:c.1493A>G	NP_001298186.1:p.Asn498Ser
XR_428840.2:n.1516+611A>G
XR_428840.4:n.1507+611A>G
NM_000506.5:c.1541A>G MANE Select	NP_000497.1:p.Asn514Ser
NM_001311257.2:c.1493A>G	NP_001298186.1:p.Asn498Ser