Canonical Allele Identifier: CA380266472
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs1360819647

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46726515G>C , CM000673.2:g.46726515G>C GRCh38
NC_000011.9:g.46748065G>C , CM000673.1:g.46748065G>C GRCh37
NC_000011.8:g.46704641G>C NCBI36
NG_008953.1:g.12323G>C , LRG_551:g.12323G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.892G>C MANE Select ENSP00000308541.5:p.Glu298Gln
ENST00000311907.9:c.892G>C ENSP00000308541.5:p.Glu298Gln
ENST00000442468.1:c.862G>C ENSP00000387413.1:p.Glu288Gln
ENST00000530231.5:c.892G>C ENSP00000433907.1:p.Glu298Gln
NM_000506.3:c.892G>C NP_000497.1:p.Glu298Gln
NM_000506.4:c.892G>C , LRG_551t1:c.892G>C NP_000497.1:p.Glu298Gln
NM_001311257.1:c.844G>C NP_001298186.1:p.Glu282Gln
XR_428840.2:n.936G>C
XR_428840.4:n.927G>C
NM_000506.5:c.892G>C MANE Select NP_000497.1:p.Glu298Gln
NM_001311257.2:c.844G>C NP_001298186.1:p.Glu282Gln