Canonical Allele Identifier: CA1969070160
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46723361T= , CM000673.2:g.46723361T= GRCh38
NC_000011.9:g.46744911T= , CM000673.1:g.46744911T= GRCh37
NC_000011.8:g.46701487T= NCBI36
NG_008953.1:g.9169T= , LRG_551:g.9169T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.423-21T= MANE Select ENSP00000308541.5:n.423-21T=
ENST00000311907.9:c.423-21T= ENSP00000308541.5:n.423-21T=
ENST00000442468.1:c.393-21T= ENSP00000387413.1:n.393-21T=
ENST00000490274.1:n.182T=
ENST00000530231.5:c.423-21T= ENSP00000433907.1:n.423-21T=
NM_000506.3:c.423-21T= NP_000497.1:n.423-21T=
NM_000506.4:c.423-21T= , LRG_551t1:c.423-21T= NP_000497.1:n.423-21T=
NM_001311257.1:c.375-21T= NP_001298186.1:n.375-21T=
XR_428840.2:n.467-21T=
XR_428840.4:n.458-21T=
NM_000506.5:c.423-21T= MANE Select NP_000497.1:n.423-21T=
NM_001311257.2:c.375-21T= NP_001298186.1:n.375-21T=