Canonical Allele Identifier: CA123015
Gene: F2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13309
ClinVar RCV Id: RCV000014236
dbSNP Id: rs387906522

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46723421_46723422insT , CM000673.2:g.46723421_46723422insT GRCh38
NC_000011.9:g.46744971_46744972insT , CM000673.1:g.46744971_46744972insT GRCh37
NC_000011.8:g.46701547_46701548insT NCBI36
NG_008953.1:g.9229_9230insT , LRG_551:g.9229_9230insT

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.462_463insT MANE Select ENSP00000308541.5:p.Asn155Ter
ENST00000311907.9:c.462_463insT ENSP00000308541.5:p.Asn155Ter
ENST00000442468.1:c.432_433insT ENSP00000387413.1:p.Asn145Ter
ENST00000490274.1:n.242_243insT
ENST00000530231.5:c.462_463insT ENSP00000433907.1:p.Asn155Ter
NM_000506.3:c.462_463insT NP_000497.1:p.Asn155Ter
NM_000506.4:c.462_463insT , LRG_551t1:c.462_463insT NP_000497.1:p.Asn155Ter
NM_001311257.1:c.414_415insT NP_001298186.1:p.Asn139Ter
XR_428840.2:n.506_507insT
XR_428840.4:n.497_498insT
NM_000506.5:c.462_463insT MANE Select NP_000497.1:p.Asn155Ter
NM_001311257.2:c.414_415insT NP_001298186.1:p.Asn139Ter