Canonical Allele Identifier: CA1969071811
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725799C= , CM000673.2:g.46725799C= GRCh38
NC_000011.9:g.46747349C= , CM000673.1:g.46747349C= GRCh37
NC_000011.8:g.46703925C= NCBI36
NG_008953.1:g.11607C= , LRG_551:g.11607C=

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-60C= MANE Select ENSP00000308541.5:p.=
ENST00000311907.9:c.560-60C= ENSP00000308541.5:p.=
ENST00000442468.1:c.530-60C= ENSP00000387413.1:p.=
ENST00000490274.1:n.340-60C=
ENST00000530231.5:c.560-60C= ENSP00000433907.1:p.=
NM_000506.3:c.560-60C= NP_000497.1:p.=
NM_000506.4:c.560-60C= , LRG_551t1:c.560-60C= NP_000497.1:p.=
NM_001311257.1:c.512-60C= NP_001298186.1:p.=
XR_428840.2:n.604-60C=
XR_428840.4:n.595-60C=
NM_000506.5:c.560-60C= MANE Select NP_000497.1:p.=
NM_001311257.2:c.512-60C= NP_001298186.1:p.=