Canonical Allele Identifier: CA1969071973
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725906A= , CM000673.2:g.46725906A= GRCh38
NC_000011.9:g.46747456A= , CM000673.1:g.46747456A= GRCh37
NC_000011.8:g.46704032A= NCBI36
NG_008953.1:g.11714A= , LRG_551:g.11714A=

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.607A= MANE Select ENSP00000308541.5:p.Ser203=
ENST00000311907.9:c.607A= ENSP00000308541.5:p.Ser203=
ENST00000442468.1:c.577A= ENSP00000387413.1:p.Ser193=
ENST00000490274.1:n.387A=
ENST00000530231.5:c.607A= ENSP00000433907.1:p.Ser203=
NM_000506.3:c.607A= NP_000497.1:p.Ser203=
NM_000506.4:c.607A= , LRG_551t1:c.607A= NP_000497.1:p.Ser203=
NM_001311257.1:c.559A= NP_001298186.1:p.Ser187=
XR_428840.2:n.651A=
XR_428840.4:n.642A=
NM_000506.5:c.607A= MANE Select NP_000497.1:p.Ser203=
NM_001311257.2:c.559A= NP_001298186.1:p.Ser187=