Canonical Allele Identifier: CA123019
Gene: F2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13312
ClinVar RCV Id: RCV000014240
dbSNP Id: rs121918484
COSMIC: COSM239762

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46726761G>A , CM000673.2:g.46726761G>A GRCh38
NC_000011.9:g.46748311G>A , CM000673.1:g.46748311G>A GRCh37
NC_000011.8:g.46704887G>A NCBI36
NG_008953.1:g.12569G>A , LRG_551:g.12569G>A

Transcript Alleles

HGVS Amino-acid change
NM_000506.3:c.1054G>A VV NP_000497.1:p.Glu352Lys
NM_000506.4:c.1054G>A , LRG_551t1:c.1054G>A NP_000497.1:p.Glu352Lys
NM_001311257.1:c.1006G>A VV NP_001298186.1:p.Glu336Lys
XR_428840.2:n.1098G>A
XR_428840.4:n.1089G>A
ENST00000311907.9:c.1054G>A ENSP00000308541.5:p.Glu352Lys
ENST00000530231.5:c.1054G>A ENSP00000433907.1:p.Glu352Lys