Canonical Allele Identifier: CA2740093696
Gene: F2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2985454
ClinVar RCV Id: RCV003848581

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46723378C>G , CM000673.2:g.46723378C>G GRCh38
NC_000011.9:g.46744928C>G , CM000673.1:g.46744928C>G GRCh37
NC_000011.8:g.46701504C>G NCBI36
NG_008953.1:g.9186C>G , LRG_551:g.9186C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.423-4C>G MANE Select ENSP00000308541.5:n.423-4C>G
ENST00000311907.9:c.423-4C>G ENSP00000308541.5:n.423-4C>G
ENST00000442468.1:c.393-4C>G ENSP00000387413.1:n.393-4C>G
ENST00000490274.1:n.199C>G
ENST00000530231.5:c.423-4C>G ENSP00000433907.1:n.423-4C>G
NM_000506.3:c.423-4C>G NP_000497.1:n.423-4C>G
NM_000506.4:c.423-4C>G , LRG_551t1:c.423-4C>G NP_000497.1:n.423-4C>G
NM_001311257.1:c.375-4C>G NP_001298186.1:n.375-4C>G
XR_428840.2:n.467-4C>G
XR_428840.4:n.458-4C>G
NM_000506.5:c.423-4C>G MANE Select NP_000497.1:n.423-4C>G
NM_001311257.2:c.375-4C>G NP_001298186.1:n.375-4C>G