Canonical Allele Identifier: CA913590875
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs1565703282

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725795_46725796del , CM000673.2:g.46725795_46725796del GRCh38
NC_000011.9:g.46747345_46747346del , CM000673.1:g.46747345_46747346del GRCh37
NC_000011.8:g.46703921_46703922del NCBI36
NG_008953.1:g.11603_11604del , LRG_551:g.11603_11604del

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-64_560-63del MANE Select ENSP00000308541.5:n.560-64_560-63del
ENST00000311907.9:c.560-64_560-63del ENSP00000308541.5:n.560-64_560-63del
ENST00000442468.1:c.530-64_530-63del ENSP00000387413.1:n.530-64_530-63del
ENST00000490274.1:n.340-64_340-63del
ENST00000530231.5:c.560-64_560-63del ENSP00000433907.1:n.560-64_560-63del
NM_000506.3:c.560-64_560-63del NP_000497.1:n.560-64_560-63del
NM_000506.4:c.560-64_560-63del , LRG_551t1:c.560-64_560-63del NP_000497.1:n.560-64_560-63del
NM_001311257.1:c.512-64_512-63del NP_001298186.1:n.512-64_512-63del
XR_428840.2:n.604-64_604-63del
XR_428840.4:n.595-64_595-63del
NM_000506.5:c.560-64_560-63del MANE Select NP_000497.1:n.560-64_560-63del
NM_001311257.2:c.512-64_512-63del NP_001298186.1:n.512-64_512-63del