Canonical Allele Identifier: CA380264755
Gene: F2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.607A>C MANE Select ENSP00000308541.5:p.Ser203Arg
ENST00000311907.9:c.607A>C ENSP00000308541.5:p.Ser203Arg
ENST00000442468.1:c.577A>C ENSP00000387413.1:p.Ser193Arg
ENST00000490274.1:n.387A>C
ENST00000530231.5:c.607A>C ENSP00000433907.1:p.Ser203Arg
NM_000506.3:c.607A>C NP_000497.1:p.Ser203Arg
NM_000506.4:c.607A>C , LRG_551t1:c.607A>C NP_000497.1:p.Ser203Arg
NM_001311257.1:c.559A>C NP_001298186.1:p.Ser187Arg
XR_428840.2:n.651A>C
XR_428840.4:n.642A>C
NM_000506.5:c.607A>C MANE Select NP_000497.1:p.Ser203Arg
NM_001311257.2:c.559A>C NP_001298186.1:p.Ser187Arg