Canonical Allele Identifier: CA1969071845
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725823A= , CM000673.2:g.46725823A= GRCh38
NC_000011.9:g.46747373A= , CM000673.1:g.46747373A= GRCh37
NC_000011.8:g.46703949A= NCBI36
NG_008953.1:g.11631A= , LRG_551:g.11631A=

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-36A= MANE Select ENSP00000308541.5:n.560-36A=
ENST00000311907.9:c.560-36A= ENSP00000308541.5:n.560-36A=
ENST00000442468.1:c.530-36A= ENSP00000387413.1:n.530-36A=
ENST00000490274.1:n.340-36A=
ENST00000530231.5:c.560-36A= ENSP00000433907.1:n.560-36A=
NM_000506.3:c.560-36A= NP_000497.1:n.560-36A=
NM_000506.4:c.560-36A= , LRG_551t1:c.560-36A= NP_000497.1:n.560-36A=
NM_001311257.1:c.512-36A= NP_001298186.1:n.512-36A=
XR_428840.2:n.604-36A=
XR_428840.4:n.595-36A=
NM_000506.5:c.560-36A= MANE Select NP_000497.1:n.560-36A=
NM_001311257.2:c.512-36A= NP_001298186.1:n.512-36A=