Canonical Allele Identifier: CA1969071813
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725801G= , CM000673.2:g.46725801G= GRCh38
NC_000011.9:g.46747351G= , CM000673.1:g.46747351G= GRCh37
NC_000011.8:g.46703927G= NCBI36
NG_008953.1:g.11609G= , LRG_551:g.11609G=

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-58G= MANE Select ENSP00000308541.5:n.560-58G=
ENST00000311907.9:c.560-58G= ENSP00000308541.5:n.560-58G=
ENST00000442468.1:c.530-58G= ENSP00000387413.1:n.530-58G=
ENST00000490274.1:n.340-58G=
ENST00000530231.5:c.560-58G= ENSP00000433907.1:n.560-58G=
NM_000506.3:c.560-58G= NP_000497.1:n.560-58G=
NM_000506.4:c.560-58G= , LRG_551t1:c.560-58G= NP_000497.1:n.560-58G=
NM_001311257.1:c.512-58G= NP_001298186.1:n.512-58G=
XR_428840.2:n.604-58G=
XR_428840.4:n.595-58G=
NM_000506.5:c.560-58G= MANE Select NP_000497.1:n.560-58G=
NM_001311257.2:c.512-58G= NP_001298186.1:n.512-58G=