Canonical Allele Identifier: CA380271597

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46729449C>G , CM000673.2:g.46729449C>G	GRCh38
NC_000011.9:g.46750999C>G , CM000673.1:g.46750999C>G	GRCh37
NC_000011.8:g.46707575C>G	NCBI36
NG_008953.1:g.15257C>G , LRG_551:g.15257C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000506.5:c.1542C>G MANE Select	NP_000497.1:p.Asn514Lys
ENST00000311907.10:c.1542C>G MANE Select	ENSP00000308541.5:p.Asn514Lys
NM_000506.3:c.1542C>G	NP_000497.1:p.Asn514Lys
NM_000506.4:c.1542C>G , LRG_551t1:c.1542C>G	NP_000497.1:p.Asn514Lys
NM_001311257.1:c.1494C>G	NP_001298186.1:p.Asn498Lys
NM_001311257.2:c.1494C>G	NP_001298186.1:p.Asn498Lys
ENST00000311907.9:c.1542C>G	ENSP00000308541.5:p.Asn514Lys
ENST00000530231.5:c.1425C>G	ENSP00000433907.1:p.Asn475Lys
XR_428840.2:n.1516+612C>G
XR_428840.4:n.1507+612C>G