Canonical Allele Identifier: CA1969071789
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs2064867532
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725782_46725793del , CM000673.2:g.46725782_46725793del GRCh38
NC_000011.9:g.46747332_46747343del , CM000673.1:g.46747332_46747343del GRCh37
NC_000011.8:g.46703908_46703919del NCBI36
NG_008953.1:g.11590_11601del , LRG_551:g.11590_11601del

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-77_560-66del MANE Select ENSP00000308541.5:n.560-77_560-66del
ENST00000311907.9:c.560-77_560-66del ENSP00000308541.5:n.560-77_560-66del
ENST00000442468.1:c.530-77_530-66del ENSP00000387413.1:n.530-77_530-66del
ENST00000490274.1:n.340-77_340-66del
ENST00000530231.5:c.560-77_560-66del ENSP00000433907.1:n.560-77_560-66del
NM_000506.3:c.560-77_560-66del NP_000497.1:n.560-77_560-66del
NM_000506.4:c.560-77_560-66del , LRG_551t1:c.560-77_560-66del NP_000497.1:n.560-77_560-66del
NM_001311257.1:c.512-77_512-66del NP_001298186.1:n.512-77_512-66del
XR_428840.2:n.604-77_604-66del
XR_428840.4:n.595-77_595-66del
NM_000506.5:c.560-77_560-66del MANE Select NP_000497.1:n.560-77_560-66del
NM_001311257.2:c.512-77_512-66del NP_001298186.1:n.512-77_512-66del
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